High-purity 2-naphthylacetonitrile and its manufacturing method

Abstract

To provide a method for producing high-purity 2-naphthylacetonitrile which contains few impurities and is useful as a raw material or intermediate for synthesizing a variety of medicinal products, agrochemicals and chemical products.SOLUTION: In the method for producing high-purity 2-naphthylacetonitrile, a reaction raw material 1 containing an acid halogen compound represented by the general formula (5) in the figure (where X represents a halogen atom), which is obtained by reacting 2-naphthylacetic acid with a halogenating agent, is mixed with a reaction raw material 2 containing sulfamide at 10°C to 100°C and heated to 85°C to 120°C to obtain 2-naphthylacetonitrile.SELECTED DRAWING: None

Description

[Technical field]

[0001] The present invention relates to high-purity 2-naphthylacetonitrile, which is useful as a raw material or intermediate for the synthesis of various pharmaceuticals, agricultural chemicals, chemical products, etc., and a method for producing the same. [Background technology]

[0002] 2-Naphthylacetonitrile is useful as a synthetic raw material or intermediate for various pharmaceuticals, agricultural chemicals, chemical products, etc. Aromatic nitrile compounds having a chemical structure similar to 2-naphthylacetonitrile are also expected to be used as synthetic raw materials or intermediates for various pharmaceuticals, agricultural chemicals, and chemical products.

[0003] For example, 2-naphthylacetonitrile is useful as a raw material or intermediate for the synthesis of pharmaceuticals such as depression (e.g., major depressive disorder, bipolar disorder), fibromyalgia, pain (e.g., neuropathic pain), sleep disorder, attention deficit disorder (ADD), attention deficit activity disorder (ADHD), restless legs syndrome, schizophrenia, anxiety, obsessive-compulsive disorder, post-traumatic stress disorder, seasonal affective disorder (SAD), premenstrual disorder, neurodegenerative diseases (e.g., Parkinson's disease, Alzheimer's disease), and other CNS diseases, diseases related to urinary incontinence and irritable bowel syndrome (IBS), and diabetes, as well as erythropoietin (EPO) inducers, calcium antagonists, histamine receptor antagonists, tachykinin receptor antagonists, 12-lipoxygenase inhibitors, protein kinase C (PKC) inhibitors, and PDEIV inhibitors.

[0004] 2-Naphthylacetonitrile can be suitably used as a raw material or intermediate for the production of (1R,5S)-1-(naphthalen-2-yl)-3-azabicyclo[3.1.0]hexane, a pharmaceutical product described in Patent Documents 1, 2, and 3, etc.

[0005] As a method for producing 2-naphthylacetonitrile, for example, a method is known in which 2-methylnaphthalene is brominated to obtain 2-(bromomethyl)naphthalene, which is then reacted with potassium cyanide to produce the compound (Non-Patent Document 1).

[0006] [ka]

[0007] However, this method is not preferable as an industrial production method because of low yields, large amounts of by-products produced by bromination, and the use of highly toxic compounds such as carbon tetrachloride and potassium cyanide.

[0008] Furthermore, a method for synthesizing a nitrile compound from an aromatic carboxylic acid or an aromatic carboxylic acid derivative has also been reported (Non-Patent Document 2). Non-Patent Document 2 describes a method in which carboxylic acid halides having various structures such as an aromatic ring and sulfamides are dissolved in sulfolane and reacted to convert them into nitrile compounds. However, the method of Non-Patent Document 2 has low yields depending on the substrate, and further improvement is required as an industrial production method.

[0009] Non-Patent Document 3 reports a method for synthesizing aromatic carboxylic acids and aromatic thioamides from aromatic ketones by the Wilgerodt reaction. However, these methods do not provide sufficient yields, and since sulfur is used in the Wilgerot reaction, it is believed that the aromatic carboxylic acids and the like produced contain a large amount of sulfur. Therefore, further improvement is required for industrial production methods. In addition, judging from the production methods and yields thereof, the 2-naphthylacetonitrile obtained by these methods is considered to contain several percent of by-products such as sulfur, amide compounds, and thioamide compounds. [Prior art documents] [Patent documents]

[0010] [Patent Document 1] WO2007 / 016155 [Patent Document 2] WO2015 / 089111 [Patent Document 3] WO2015 / 102826 [Non-patent literature]

[0011] [Non-Patent Document 1] Tetrahedron Letters 56 (2015) 2054-2058 [Non-Patent Document 2] Tetrahedron Letters, Vol.23, No.14, pp.1505-1508, 1982 [Non-Patent Document 3] Synthetic Communications, Vol.33, No.1, pp.59-63, 2003 Summary of the Invention [Problem to be solved by the invention]

[0012] The present invention provides a method for producing high-purity 2-naphthylacetonitrile which has few impurities, is safe, highly efficient, and can be produced inexpensively on an industrial scale. [Means for solving the problem]

[0013] In order to solve the above problems, the present inventors have discovered a method for producing an aromatic carboxylic acid compound such as 2-naphthylacetic acid from a relatively inexpensive and versatile aromatic ketone compound such as 2'-acetonaphthone by utilizing the Wilgerot rearrangement, and further a method for producing an aromatic nitrile compound such as 2-naphthylacetonitrile in high yield and with high purity from the aromatic carboxylic acid compound (International Application No. PCT / JP2019 / 018065). Generally, high purity is required for raw materials and intermediates for the synthesis of pharmaceuticals so that unexpected side effects due to impurities contained therein do not occur. Examples of impurities include by-products generated during the production of these. Although by-products may be removable during purification or the manufacturing process of the target pharmaceutical, when pharmaceuticals are manufactured industrially and in large quantities, it is desirable to reduce manufacturing and purification costs in order to ensure a stable supply of pharmaceuticals and to suppress prices, and therefore high-purity raw materials and intermediates for the synthesis of pharmaceuticals with fewer impurities are desired. As a result of investigations, the present inventors found that the 2-naphthylacetonitrile obtained by the production method described in the above-mentioned international application has a lower content of by-products than that obtained by the conventionally known methods, and thus arrived at the present invention. The present inventors further investigated this production method.

[0014] That is, the gist of the present invention is as follows. [1] High-purity 2-naphthylacetonitrile having an HPLC purity of 95 area % or more and containing one or more naphthalene compounds represented by the following formulas (a) to (j) as impurities, the contents of each naphthalene compound being as follows:

[0015] [ka]

[0016] [2] The high-purity 2-naphthylacetonitrile according to [1], containing one or more impurities selected from the naphthalene compounds represented by the following formulas (a) to (d), in which the contents of each naphthalene compound are as follows:

[0017] [ka]

[0018] [3] The high-purity 2-naphthylacetonitrile according to [1], which contains a naphthalene compound represented by the following formula (c) as an impurity, and the content of the naphthalene compound represented by the formula (c) is 1 area % or less.

[0019] [ka]

[0020] [4] The following general formula (5)

[0021] [ka]

[0022] (In the general formula (5), X represents a halogen atom.) and a first organic solvent, and a reaction raw material 2 containing sulfamide and a second organic solvent are mixed at 15°C to 90°C, and the mixture is heated to 80°C to 180°C to react with each other to obtain high-purity 2-naphthylacetonitrile. [5] A method for producing high-purity 2-naphthylacetonitrile according to [4], characterized in that reactant 1 is added to reactant 2 at 15°C to 90°C, and the mixture is heated to 80°C to 180°C for reaction. [6] For 1 mole of sulfamide,

[0023] [ka]

[0024] The method for producing high-purity 2-naphthylacetonitrile according to [5], characterized in that the reaction material 1 is added to the reaction material 2 so that the amount of the acid halide compound represented by the formula (I) is 0.0027 mol / min or more. [7] The method for producing high-purity 2-naphthylacetonitrile according to any one of [4] to [6], wherein the reaction raw material 1 is obtained by mixing 2-naphthylacetic acid, a halogenating agent and a first organic solvent, optionally in the presence of a catalyst. [8] A method for producing high-purity 2-naphthylacetonitrile, comprising the following steps 1 and 2: Step 1: a step of subjecting 2'-acetonaphthone to a Wilgerott reaction in the presence of an additive, if necessary, to a reaction to obtain an amide compound, hydrolyzing the resulting amide compound, and then liberating 2-naphthylacetic acid to obtain 2-naphthylacetic acid; Step 2: A process for obtaining 2-naphthylacetonitrile by mixing and reacting a reaction raw material 1 containing 2-naphthylacetic acid obtained in the process 1, a halogenating agent, and a first organic solvent with a reaction raw material 2 containing sulfamide and a second organic solvent. [9] The method for producing high-purity 2-naphthylacetonitrile according to any one of [4] to [7], characterized in that the first organic solvent is a hydrocarbon solvent, an amide solvent, a sulfone solvent or a mixed solvent thereof, and the second organic solvent is a sulfone solvent.

[0025] The present invention also relates to the following: [1A] High-purity 2-naphthylacetonitrile, having an HPLC purity of 95 area % or more and containing the following naphthalene compounds represented by the following formulas (a) to (i):

[0026] [ka]

[0027] [2A] A method for producing high-purity 2-naphthylacetonitrile, comprising the following steps 1A and 2A: Process 1A: a step of subjecting 2'-acetonaphthone to a Wilgerott reaction in the presence of an additive, if necessary, to a reaction to obtain an amide compound, followed by hydrolysis and neutralization to obtain 2-naphthylacetic acid; Process 2A: The 2-naphthylacetic acid obtained in step 1A, a halogenating agent, and a compound represented by the following general formula (7) R 1 SO2R 2 (7) (In the formula, R 1 and R 2 each independently represents a chlorine atom, a hydroxyl group, an amino group, an isocyanate group, or a p-tolyl group. In a step of reacting a compound represented by the formula (I) in an organic solvent, optionally in the presence of a catalyst, to obtain 2-naphthylacetonitrile.

[0028] [3A] The step 2A is A method for producing high-purity 2-naphthylacetonitrile according to [2A], characterized in that it is a step of mixing and reacting a reaction raw material 1 obtained by mixing 2-naphthylacetic acid obtained in step 1A, a halogenating agent, a first organic solvent, and a catalyst as necessary, with a reaction raw material 2 obtained by mixing a compound represented by the general formula (7) and a second organic solvent to obtain 2-naphthylacetonitrile.

[0029] [4A] The method for producing high-purity 2-naphthylacetonitrile according to [3A], characterized in that the first organic solvent is a hydrocarbon solvent, a sulfone solvent or a mixture thereof, and the second organic solvent is a sulfone solvent.

[0030] [5A] The step 2A is The method for producing high-purity 2-naphthylacetonitrile described in [3A] is characterized in that it is a step of mixing a reaction raw material 1 obtained by mixing 2-naphthylacetic acid obtained in step 1A, a halogenating agent, a first organic solvent, and a catalyst as necessary, with a reaction raw material 2 obtained by mixing a compound represented by the general formula (7) and a second organic solvent at 15°C to 90°C, and then heating the mixture to react at 80°C to 180°C to obtain 2-naphthylacetonitrile.

[0031] [6A] The step 2A A process for obtaining 2-naphthylacetonitrile by adding a reaction raw material 1 obtained by mixing 2-naphthylacetic acid obtained in step 1A, a halogenating agent, a first organic solvent, and, if necessary, a catalyst, to a reaction raw material 2 obtained by mixing a compound represented by the general formula (7) and a second organic solvent, and reacting the mixture, The compound represented by the general formula (7) contained in the reaction raw material 2 is mixed with 1 mol of the compound represented by the following general formula (5) contained in the reaction raw material 1.

[0032] [ka]

[0033] (In the general formula (5), X represents a halogen atom.) The method for producing high-purity 2-naphthylacetonitrile according to [3A], characterized in that the reaction material 1 is added to the reaction material 2 so that the amount of the acid halide compound represented by the following formula is 0.0027 mol / min or more.

[0034] [7A] A method for producing high-purity 2-naphthylacetonitrile according to [2A], characterized in that in step 1A, after the hydrolysis, the reaction product obtained by the hydrolysis is contacted with a hydrocarbon solvent, a hydrocarbon solvent is present during the neutralization, or the reaction product obtained by the neutralization is contacted with a hydrocarbon solvent. Effect of the Invention

[0035] According to the present invention, it is possible to provide high-purity 2-naphthylacetonitrile with few impurities, which is useful as a raw material or intermediate for synthesizing various pharmaceuticals, agricultural chemicals, and chemical products, particularly as a raw material or intermediate for synthesizing pharmaceuticals. It is also possible to provide a method for producing high-purity 2-naphthylacetonitrile that is safe, highly efficient, and can be produced industrially and in large quantities at low cost. Furthermore, by using the 2-naphthylacetonitrile of the present invention, pharmaceuticals such as (1R,5S)-1-(naphthalen-2-yl)-3-azabicyclo[3.1.0]hexane can be produced industrially and in large quantities at low cost. [Brief description of the drawings]

[0036] [Figure 1] FIG. 1 shows the results of HPLC analysis of 2-naphthylacetonitrile obtained in Example 1. [Diagram 2] FIG. 2 shows the results of HPLC analysis of 2-naphthylacetonitrile obtained in Example 3. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0037] The present invention will be described in detail below. High-purity 2-naphthylacetonitrile of the present invention The high-purity 2-naphthylacetonitrile of the present invention has a lower content of specific by-products (impurities) than conventional products. Specifically, the HPLC purity of 2-naphthylacetonitrile is 95 area % or more, and the content of the naphthalene compounds represented by the following formulas (a) to (j) is as shown in Table 1.

[0038] [Table 1]

[0039] The compounds represented by the above formulas (a), (b), (c), (d) and (h) are impurities that are difficult to remove by purification procedures such as solid-liquid separation by crystallization or column purification, and it is preferable to suppress the amount of production from the viewpoints of quality and purification costs. The compounds represented by the above formulas (e), (f), (g), (i) and (j) are highly reactive and may cause side reactions, so it is preferable that they are not allowed to remain in 2-naphthylacetonitrile. The HPLC purity of the high purity 2-naphthylacetonitrile of the present invention is preferably 97 area % or more, more preferably 98 area % or more, and particularly preferably 99 area % or more. The content of the naphthalene compound represented by the above formula (a) is preferably 0.25 area % or less, more preferably 0.2 area % or less, further preferably 0.15 area % or less, and particularly preferably 0.1 area % or less. The contents of the naphthalene compounds represented by the above formulas (b) and (d) are each preferably 0.08 area % or less, more preferably 0.05 area % or less, even more preferably 0.03 area % or less, and particularly preferably 0.01 area % or less. The content of the naphthalene compound represented by the above formula (c) is preferably 0.8 area % or less, more preferably 0.5 area % or less, further preferably 0.3 area % or less, and particularly preferably 0.1 area % or less. The contents of the naphthalene compounds represented by the above formulas (e), (f) and (h) are each preferably 0.03 area % or less, more preferably 0.02 area % or less, even more preferably 0.01 area % or less, and particularly preferably 0.005 area % or less. The content of the naphthalene compound represented by the above formula (g) is preferably 0.08 area % or less, more preferably 0.05 area % or less, further preferably 0.03 area % or less, and particularly preferably 0.01 area % or less. The content of the naphthalene compounds represented by the above formulas (i) and (j) is preferably 0.03 area % or less, more preferably 0.02 area % or less, further preferably 0.01 area % or less, and particularly preferably 0 area %. The content of the naphthalene compound represented by the following formula is preferably 0.08 area % or less, more preferably 0.05 area % or less, further preferably 0.03 area % or less, and particularly preferably 0.01 area % or less.

[0040] [ka]

[0041] The high-purity 2-naphthylacetonitrile of the present invention has a low impurity content and can be used as it is as a raw material / intermediate for the synthesis of pharmaceuticals without purification procedures, etc., and is therefore useful as a raw material / intermediate for the synthesis of pharmaceuticals. Among the impurities in the high purity 2-naphthylacetonitrile of the present invention, the naphthalene compound represented by the above formula (c) which is contained in the greatest amount, can be inhibited from being produced by the production method of the present invention described below. The relative retention times (RRT) of the naphthalene compounds represented by the above formulas (a) to (h) are shown in Table 2. The relative retention times may vary by about ±0.05 depending on the HPLC measurement conditions.

[0042] [Table 2]

[0043] In the present invention, the purity of 2-naphthylacetonitrile and the content of impurities can be measured by the peak area ratio in high performance liquid chromatography (HPLC), which is a method well known in the field of analytical chemistry. The measurement conditions for HPLC can be appropriately selected, but the following conditions are preferable. Analytical equipment: Agilent HPLC (1200 series) Column: Zorbax Eclipse Plus Phenyl-Hexyl, 5 μm, 250 mm × 4.6 mm Mobile phase A: 0.1% by volume trifluoroacetic acid aqueous solution Mobile phase B: Acetonitrile Gradient: 0 min (B: 30%) - 15 min (B: 60%) - 20 min (B: 95%) - 30 min (B: 95%) Flow rate: 1.0 mL / min Injection volume: 5 μL Detection wavelength: 280 nm Column temperature: 40℃

[0044] The color tone of the high purity 2-naphthylacetonitrile of the present invention is white to brown, preferably white to light brown. The water content of the high purity 2-naphthylacetonitrile of the present invention is usually 2.0% by weight or less, preferably 1.5% by weight or less, more preferably 1.0% by weight or less. In addition, the high purity 2-naphthylacetonitrile of the present invention uses sulfur and an organic solvent in the manufacturing process, but the content of these is also low. The sulfur content of the high purity 2-naphthylacetonitrile of the present invention is usually 0.5 area % or less, preferably 0.3 area % or less, more preferably 0.1 area % or less, and particularly preferably 0.05 area % or less. The content of an organic solvent such as sulfolane or toluene is usually 0.5 weight % or less, preferably 0.3 weight % or less, more preferably 0.1 weight % or less, and particularly preferably 0.05 weight % or less. As described above, the high-purity 2-naphthylacetonitrile of the present invention has a high HPLC purity of 95 area % or more, more preferably 98 area % or more, and contains less impurities than 2-naphthylacetonitrile produced by conventional methods, so that high reactivity can be expected when used as a raw material / intermediate for the synthesis of pharmaceuticals. In addition, the high-purity 2-naphthylacetonitrile of the present invention has excellent solubility and a high dissolution rate in organic solvents. Therefore, the high-purity 2-naphthylacetonitrile of the present invention is useful as a raw material / intermediate for the synthesis of pharmaceuticals produced in large quantities industrially.

[0045] The method for producing high-purity 2-naphthylacetonitrile according to the present invention The method for producing high-purity 2-naphthylacetonitrile of the present invention includes a step (step 1) of obtaining 2-naphthylacetic acid represented by the following formula (3) from 2'-acetonaphthone represented by the following formula (2), and a step (step 2) of obtaining 2-naphthylacetonitrile represented by the following formula (1) from 2-naphthylacetic acid.

[0046] [ka]

[0047] <<Process 1>> Step 1 is a step in which 2'-acetonaphthone represented by formula (2) is subjected to the Wilgerot reaction, and then the resulting compound is hydrolyzed to obtain 2-naphthylacetic acid represented by formula (3). In this specification, the Wilgerot reaction means the Wilgerot reaction and the Wilgerot-Kindler reaction.

[0048] [Wilgerott reaction] The Wilgerott reaction can be carried out by reacting 2'-acetonaphthone with a sulfur compound such as sodium sulfide (Na2S·9H2O) or ammonium sulfide ((NH4)2S) under heating. [Wilgerott-Kindler reaction] The Wilgerodt-Kindler reaction can be carried out by reacting 2'-acetonaphthone with sulfur and a secondary amine such as a dialkylamine or morpholine under heating.

[0049] <Raw materials> (2'-Acetonaphthone) As the 2'-acetonaphthone, a commercially available product may be used, or a product obtained by a known method may be used. (Sulfur compounds) The sulfur compounds may be used alone or in any combination and ratio of two or more kinds. The amount of the sulfur compound used is not particularly limited as long as it is an amount effective for the Wilgerott reaction of 2'-acetonaphthone. The amount of the sulfur compound used is usually 1 mol to 5 mol, preferably 1 mol to 3 mol, per mol of 2'-acetonaphthone. (sulfur) The amount of sulfur used is not particularly limited as long as it is an amount effective for the reaction, but is usually 1 mol to 5 mol, and preferably 1 mol to 3 mol, per mol of 2'-acetonaphthone. (Secondary amine) As the secondary amine, morpholine is preferred for industrial production because the reaction can be efficiently carried out without a solvent. The amount of the secondary amine used is not particularly limited as long as it is an amount effective for the reaction. The amount of the secondary amine used is usually 1 mol to 6 mol, preferably 2 mol to 4 mol, per mol of 2'-acetonaphthone. (solvent) Step 1 can be carried out without a solvent or in an organic solvent inert to the reaction. Examples of the organic solvent include dioxane and N,N-dimethylformamide. These organic solvents may be used alone or in any combination and ratio of two or more. When a reaction is carried out using a sulfur compound, the reaction can be carried out in the presence of an aqueous solvent such as water.

[0050] (Additives) In step 1, an additive may be used, if necessary. The additives include dehydrating agents such as zeolite, molecular sieves, magnesium sulfate, or sodium sulfate. The dehydrating agents may be used alone or in any combination and ratio of two or more. The reaction can be efficiently carried out by controlling the amount of water in the reaction system to be low using the dehydrating agent. The amount of the dehydrating agent used is not particularly limited as long as the dehydration proceeds efficiently, but is usually 1 mol to 5 mol, and preferably 1.5 mol to 4 mol, per mol of 2'-acetonaphthone. Examples of additives include organic acids such as p-toluenesulfonic acid, methanesulfonic acid, oxalic acid, and trifluoroacetic acid. The organic acids may be used alone or in any combination and ratio of two or more. As the organic acids, p-toluenesulfonic acid and methanesulfonic acid are particularly preferred. By using these additives, by-products, particularly compounds represented by the following formula, are reduced.

[0051] [ka]

[0052] In this way, the formation of a ketothioamide compound represented by the following formula (1) is suppressed, and the reaction can proceed efficiently. The amount of the organic acid used is usually 0.01 mol to 5 mol, and preferably 0.05 mol to 3 mol, per mol of 2'-acetonaphthone. In order to control the amount of water in the reaction system to be small, the reaction may be carried out while removing water by distillation.

[0053] <Reaction conditions> (Reaction method) The production method of the present invention may be a batch type or a continuous type, but is usually carried out in a batch type. (Reaction temperature) The reaction temperature is usually 90°C to 150°C, preferably 100°C to 140°C, and particularly preferably 110°C to 130°C. (Reaction pressure) The reaction is usually carried out under normal pressure, but may be carried out under increased pressure. (Reaction time) The reaction time can be appropriately selected depending on the progress of the reaction, and is usually 1 to 24 hours, preferably 2 to 12 hours.

[0054] <Post-processing> [Hydrolysis] After the Wilgerott reaction, the resulting compound may be separated from the reaction system and then subjected to hydrolysis, or may be subjected to the next hydrolysis without being separated.

[0055] In the present invention, after the Wilgerott reaction, the resulting compound can be hydrolyzed with a base. (base) Examples of the base include alkali metal hydroxides such as sodium hydroxide and potassium hydroxide; alkaline earth metal hydroxides such as calcium hydroxide; alkali metal carbonates such as sodium carbonate and potassium carbonate; alkaline earth metal carbonates such as calcium carbonate; alkali metal hydrogen carbonates such as sodium hydrogen carbonate and potassium hydrogen carbonate; alkaline earth metal hydrogen carbonates such as calcium hydrogen carbonate; and alkali metal alkoxides such as sodium methoxide, sodium ethoxide, potassium methoxide, and potassium ethoxide. From the viewpoint of cost and availability, it is preferable to use alkali metal hydroxides such as sodium hydroxide and potassium hydroxide industrially. One type of base may be used alone, or two or more types may be used in any combination and ratio. The amount of the base used is not particularly limited as long as it is an amount effective for hydrolyzing the compound obtained after the Wilgerott reaction. The amount of the base used is preferably 1 mol to 10 mol, preferably 1 mol to 5 mol, per mol of the compound obtained after the Wilgerott reaction. (solvent) The hydrolysis may be carried out without a solvent or in a solvent such as water, but is preferably carried out in a solvent from the viewpoint of excellent stirrability and uniformity. (Reaction temperature) The reaction temperature for hydrolysis is not particularly limited as long as the hydrolysis proceeds at the temperature. The reaction temperature for hydrolysis is usually 80°C to 115°C, and preferably 85°C to 110°C. (Reaction pressure) The hydrolysis is usually carried out under normal pressure, but may be carried out under increased pressure.

[0056] [Release reaction] The reaction product obtained by hydrolysis (for example, 2-naphthylacetic acid or a salt thereof) can be reacted with an acid to liberate 2-naphthylacetic acid represented by formula (3). (acid) To effect the reaction to liberate 2-naphthylacetic acid, an acid such as hydrochloric acid, sulfuric acid, or hydrobromic acid can be used. The acid may be used alone or in any combination and ratio of two or more kinds. From the viewpoints of reaction efficiency, cost, etc., hydrochloric acid is industrially preferred. The amount of the acid used is not particularly limited as long as it is an amount effective for neutralization. The amount of the acid used is usually 1 mol to 20 mol, preferably 3 mol to 10 mol, per mol of the reaction product obtained by hydrolysis.

[0057] <Reaction conditions> (humoral) The pH of the mixture during the reaction to liberate 2-naphthylacetic acid is usually 0 to 5, and preferably 0 to 3. (Reaction temperature) The temperature of the liberation reaction is not particularly limited as long as the liberation proceeds at the temperature. The temperature of the liberation reaction is usually 50°C to 90°C, and preferably 60°C to 80°C. (Reaction time) The reaction time is usually 10 minutes to 5 hours, preferably 30 minutes to 2 hours. (Reaction pressure) The reaction pressure is usually normal pressure, but may be increased. (Supply method) The supply method may be to supply the reaction product obtained by hydrolysis as a bed liquid to the reactor and then supply the acid, or to supply the reaction product obtained by hydrolysis as a bed liquid to the reactor and then supply the acid, or to supply the reaction product obtained by hydrolysis and the acid simultaneously.

[0058] <Post-processing> 2-Naphthylacetic acid can be extracted and recovered from the reaction product obtained by the liberation reaction using an organic solvent. (Organic solvent) The organic solvent may be a hydrocarbon solvent capable of dissolving 2-naphthylacetic acid. Examples of the hydrocarbon solvent include alicyclic hydrocarbon solvents such as cyclohexane and methylcyclohexane; aromatic hydrocarbon solvents such as benzene, toluene, xylene, mesitylene, ethylbenzene, and tert-butylbenzene; and aromatic halogenated hydrocarbon solvents such as trifluoromethylbenzene, nitrobenzene, chlorobenzene, chlorotoluene, and bromobenzene. From the viewpoint of cost, the hydrocarbon solvent is preferably an alicyclic hydrocarbon solvent or an aromatic hydrocarbon solvent, and more preferably cyclohexane, toluene, and xylene. The hydrocarbon solvents may be used alone or in combination of two or more kinds in any desired ratio. The amount of the organic solvent used is usually 1 to 20 times, preferably 1.5 to 10 times, and particularly preferably 3 to 5 times, the volume of 2-naphthylacetic acid.

[0059] (purification method) Since sulfur or a sulfur compound is used in step 1, the resulting reaction product usually contains several mol % or more of sulfur. Sulfur is an impurity for 2-naphthylacetic acid, which is the target product of step 1, and may also reduce the reaction efficiency when chemical reactions are carried out using 2-naphthylacetic acid as a raw material, so it is preferable to remove sulfur as much as possible. In the present invention, the sulfur content of 2-naphthylacetic acid obtained in step 1 can be reduced by contacting the reaction product obtained by hydrolysis with a hydrocarbon solvent after the hydrolysis, by making a hydrocarbon solvent present during the liberation, or by contacting the reaction product obtained by the liberation with a hydrocarbon solvent. When contacting with a hydrocarbon solvent, water or an aqueous solution may be present as necessary. When contacting with a hydrocarbon solvent, the amount of the hydrocarbon solvent used is usually 1 to 30 times by volume, preferably 3 to 20 times by volume, and particularly preferably 5 to 15 times by volume relative to 2-naphthylacetic acid.

[0060] In the present invention, since the removal of sulfur and the extraction of 2-naphthylacetic acid can be carried out using a single solvent, toluene is particularly preferred as the hydrocarbon solvent. As described above, in step 1 of the present invention, 2-naphthylacetic acid obtained by contacting with a hydrocarbon solvent or the like is of high quality having a sulfur content of 0.001 mol% to 1 mol%, preferably 0.001 mol% to 0.5 mol%, and a purity of 98 mol% or more, preferably 99 mol% or more. (Isolation method) The reaction product obtained by the liberation reaction may be added with an organic solvent capable of dissolving 2-naphthylacetic acid (e.g., toluene, xylene, cyclohexane, etc.), washed once or multiple times with an appropriate washing liquid such as water or an aqueous solution, and isolated using a known method. For example, the mixture is stirred under acidic conditions (e.g., pH 3 or less) and at elevated temperatures (e.g., 50°C to 90°C), washed as necessary, separated the aqueous layer, concentrated, etc., and then cooled to precipitate and recover 2-naphthylacetic acid as a solid. The 2-naphthylacetic acid obtained in step 1 is useful as a synthetic raw material or synthetic intermediate for various industrial products, pharmaceuticals, etc., and can also be subjected to step 2 of the present invention.

[0061] <<Process 2>>

[0062] [ka]

[0063] (In the formula, X is a halogen atom.)

[0064] Step 2 is a step of obtaining 2-naphthylacetonitrile represented by formula (1), which includes the following two reactions I and II. Reaction I: A reaction in which 2-naphthylacetic acid represented by formula (4) and a halogenating agent are mixed in a first organic solvent, optionally in the presence of a catalyst, to obtain a reaction raw material 1 containing a compound represented by formula (5). Reaction II: A reaction in which a raw material 1 containing the compound represented by formula (5) and a raw material 2 containing sulfamide and a second organic solvent are mixed to obtain 2-naphthylacetonitrile.

[0065] [Reaction I] This is a reaction in which 2-naphthylacetic acid represented by formula (3) and a halogenating agent are mixed in a first organic solvent, optionally in the presence of a catalyst, to obtain a reaction raw material 1 containing a compound represented by formula (5).

[0066] [ka]

[0067] (In the formula, X is a halogen atom.)

[0068] <Raw materials> (2-Naphthylacetic acid) As the 2-naphthylacetic acid, the one obtained in the above step 1 or a commercially available one can be used.

[0069] (Halogenating Agent) The halogenating agent is not particularly limited as long as it can halogenate 2-naphthylacetic acid. As the halogenating agent, a chlorinating agent and a brominating agent are preferable, and a chlorinating agent is more preferable. The chlorinating agent includes thionyl chloride, oxalyl chloride, sulfuryl chloride, phosphoryl chloride, phosphorus trichloride, phosphorus pentachloride, and the like. The brominating agent includes thionyl bromide, phosphorus tribromide, and the like. Among these, thionyl chloride, phosphoryl chloride, phosphorus pentachloride, thionyl bromide, and phosphorus tribromide are preferred, and thionyl chloride is particularly preferred, from the viewpoints of cost, versatility, reactivity, etc. These halogenating agents may be used alone or in any combination and ratio of two or more kinds. The amount of the halogenating agent used is not particularly limited as long as it is an amount capable of halogenating 2-naphthylacetic acid. In order to sufficiently halogenate 2-naphthylacetic acid, it is usually preferable to use 1 mol or more of the halogenating agent per 1 mol of 2-naphthylacetic acid. The upper limit of the amount used is not particularly limited, but from the viewpoints of cost, productivity, etc., it is preferably 3 mol or less per 1 mol of 2-naphthylacetic acid.

[0070] (catalyst) Reaction I can be carried out in the presence of a catalyst as necessary. The catalyst is not particularly limited as long as it promotes the reaction, but it is preferable to carry out the reaction in the presence of a catalyst in order to increase the reactivity. Examples of the catalyst include tertiary amides such as N,N-dimethylformamide, N,N-dimethylacetamide, and N-methylpyrrolidinone. N,N-dimethylformamide is particularly preferred because it is easily available and inexpensive. The amount of the catalyst used is not particularly limited as long as it is an amount effective for functioning as a catalyst, and is preferably 0.0001 mol to 1 mol, more preferably 0.001 mol to 0.1 mol, per mol of 2-naphthylacetic acid.

[0071] (First organic solvent) The first organic solvent is not particularly limited as long as the reaction proceeds. Examples of the first organic solvent include hydrocarbon solvents, amide solvents, sulfoxide solvents, and sulfone solvents. These organic solvents may be used alone or in any combination and ratio of two or more. Examples of the hydrocarbon solvent that can be used include chain aliphatic hydrocarbons such as hexane and heptane; cyclic aliphatic hydrocarbons such as cyclohexane, methylcyclohexane and cycloheptane; aromatic hydrocarbons such as benzene, toluene, xylene, mesitylene, ethylbenzene and tert-butylbenzene; and aromatic halogenated hydrocarbons such as trifluoromethylbenzene, nitrobenzene, chlorobenzene, chlorotoluene and bromobenzene. As the amide solvent, for example, aprotic amides such as N,N-dimethylformamide, N,N-dimethylacetamide, and N-methylpyrrolidinone can be used, and N,N-dimethylformamide is preferred. As the sulfoxide solvent, for example, an aprotic sulfoxide such as dimethyl sulfoxide can be used. As the sulfone solvent, for example, aprotic sulfone such as ethyl methyl sulfone, ethyl isopropyl sulfone, 3-methyl sulfolane, sulfolane, etc. can be used, and sulfolane is preferred. As the first organic solvent, from the viewpoints of excellent operability, productivity, and the like, and cost, and the like, a hydrocarbon solvent, an amide solvent, or a sulfone solvent is preferable, a hydrocarbon solvent or an amide solvent is more preferable, and among them, toluene, xylene, chlorobenzene, and N,N-dimethylformamide are more preferable, and toluene is particularly preferable. Furthermore, from the viewpoints of excellent reactivity, operability, productivity, etc., and cost, etc., it is also preferable to use a mixture of a hydrocarbon solvent and an amide solvent as the first organic solvent, and in particular, a mixture of toluene and N,N-dimethylformamide is preferable. The mixing ratio (volume ratio) of the hydrocarbon solvent and the amide solvent can be appropriately selected within the range of 1:99 to 99:1. The amount of the first organic solvent used is usually 1 L or more, and from the viewpoints of operability and the like, preferably 2 L or more, and more preferably 3 L or more, relative to 1 kg of 2-naphthylacetic acid. The upper limit, from the viewpoints of operability, productivity, cost, and the like, is usually 50 L or less, preferably 30 L or less, more preferably 20 L or less, even more preferably 10 L or less, particularly preferably 4.5 L or less, and most preferably 4 L or less. (Inorganic additives) In the reaction I, an inorganic additive (e.g., diatomaceous earth, silicic anhydride, silicon dioxide, sodium sulfate, magnesium sulfate, sodium chloride, magnesium chloride, calcium carbonate, magnesium carbonate, etc.) may be added as necessary. By using the inorganic additive, the reaction can proceed smoothly.

[0072] <Reaction conditions> (Reaction temperature) The reaction temperature is usually 15° C. to 70° C., preferably 20° C. to 65° C., and particularly preferably 30° C. to 60° C. If the reaction temperature is too low, the reaction may proceed slowly, resulting in reduced productivity, whereas if the reaction temperature is too high, by-products may be produced, resulting in reduced quality. (Reaction time) The reaction time is usually 0.5 to 30 hours, preferably 1 to 15 hours, and particularly preferably 2 to 10 hours. (Reaction pressure) The reaction pressure is usually normal pressure, but the reaction may be carried out under increased pressure.

[0073] <Post-processing> When the reaction liquid obtained in reaction I containing the compound represented by formula (5) is used in reaction II, the reaction liquid may be used as it is, or a concentrated liquid obtained by concentrating the reaction liquid may be used, or the organic layer obtained by mixing the reaction liquid with water or an aqueous alkali solution to neutralize it and separating it may be used, or a poor solvent may be added to the organic layer to cause crystallization and then a treatment such as filtration may be used. Furthermore, the product obtained in reaction I may be purified by a known purification means such as column chromatography. In the production method of the present invention, from the viewpoint of cost and productivity, it is preferable to use the reaction liquid or the concentrated liquid as it is in reaction II.

[0074] [Reaction II] This is a reaction in which a compound represented by formula (5), sulfamide, and a second organic solvent are mixed to obtain 2-naphthylacetonitrile represented by formula (1).

[0075] [ka]

[0076] (In the formula, X is a halogen atom.) This reaction II can suppress the production of the naphthalene compound (by-product) described in the section "High-purity 2-naphthylacetonitrile of the present invention."

[0077] <Raw materials> (Compound represented by formula (5)) As the compound represented by formula (5), the compound obtained in reaction I can be used, and from the viewpoint of productivity, it is preferable to use a concentrate obtained by concentrating the reaction solution obtained in reaction I. (Sulfamide) Sulfamides that can be used are commercially available. The amount of sulfamide used is usually 1 mol or more per mol of 2-naphthylacetic acid, and is usually 1 mol to 5 mol, preferably 1.02 mol to 3 mol, more preferably 1.03 mol to 2 mol, and particularly preferably 1.05 mol to 1.5 mol, per mol of 2-naphthylacetic acid. (Second organic solvent) The second organic solvent may be the same as the first organic solvent described above, but is preferably a sulfone solvent, and more preferably sulfolane from the standpoint of reactivity, productivity, and the like. Furthermore, it is also preferable to use a mixture of a hydrocarbon solvent and a sulfone solvent as the second organic solvent, and in particular, a mixture of toluene and sulfolane is preferable. The mixing ratio (volume ratio) of the hydrocarbon solvent and the sulfone solvent can be appropriately selected within the range of 1:99 to 99:1. The amount of the second organic solvent used is usually 1 L or more, and from the viewpoints of operability and the like, preferably 2 L or more, and more preferably 3 L or more, relative to 1 kg of 2-naphthylacetic acid. The upper limit, from the viewpoints of operability, productivity, cost, and the like, is usually 50 L or less, preferably 30 L or less, more preferably 20 L or less, even more preferably 4.5 L or less, and particularly preferably 4 L or less. (Inorganic additives) In the reaction II, an inorganic additive (e.g., diatomaceous earth, silicic anhydride, silicon dioxide, sodium sulfate, magnesium sulfate, sodium chloride, magnesium chloride, calcium carbonate, magnesium carbonate, etc.) may be added as necessary. By using the inorganic additive, the reaction can proceed smoothly.

[0078] <Reaction conditions> (Reaction temperature) The reaction temperature may vary depending on the organic solvent and catalyst used, etc., but the lower limit is usually 80°C or higher, preferably 85°C or higher, and particularly preferably 90°C or higher, from the viewpoints of quality, reactivity, cost, etc., and the upper limit is usually 180°C or lower, preferably 150°C or lower, more preferably 120°C or lower, and particularly preferably 110°C or lower, from the viewpoints of quality, reactivity, cost, etc. If the reaction temperature is too low, the reaction may proceed slowly, resulting in a decrease in productivity, whereas if the reaction temperature is too high, by-products may be produced, resulting in a decrease in the yield and quality of the target 2-naphthylacetonitrile. In this embodiment, after mixing the reaction raw materials 1 and 2, the temperature may be raised to 80° C. to 180° C. to cause a reaction, or the reaction raw materials 1 at 80° C. to 180° C. may be mixed with the reaction raw materials 2 at 80° C. to 180° C. to cause a reaction. Furthermore, the reaction raw materials 2 may be added to the reaction raw materials 1 and mixed, or the reaction raw materials 1 may be added to the reaction raw materials 2 and mixed. (Reaction time) The reaction time of reaction raw materials 1 and 2 may vary depending on the halogenating agent, organic solvent, catalyst, etc. used, but can be appropriately selected depending on the progress of the reaction, and is usually 0.5 to 48 hours, preferably 1 to 24 hours, and particularly preferably 2 to 12 hours. When the reaction proceeds from the start of mixing reaction raw materials 1 and 2, the reaction time means the time from the start of mixing to the start of post-treatment. (Reaction pressure) The pressure during the reaction is usually normal pressure, but may be increased.

[0079] (Reaction method) The production method of the present invention may be a batch type or a continuous type, but is usually carried out in a batch type. (supply order) The order of supplying the reactants 1 and 2 can be appropriately selected. For example, the reactants 1 may be used as a bed liquid to supply the reactants 2 to one reactor and then mixed, or the reactants 1 may be used as a bed liquid to supply the reactants 2 to one reactor and then mixed, or the reactants 1 and 2 may be simultaneously supplied and mixed. By setting the temperature of the mixture of reactant 1 and reactant 2 to a temperature relatively lower than the reaction temperature, the generation of by-products due to over-reaction is suppressed, and 2-naphthylacetonitrile of higher purity can be produced efficiently and at low cost even in industrial-scale mass synthesis. (Supply method) Examples of the supply method include a method in which the entire amount of reaction raw material 1 is added to reaction raw material 2 at once, a method in which reaction raw material 1 is divided into two or more portions and added in two or more portions with a time interval therebetween, and a method in which a constant amount is added intermittently or continuously by dropwise addition, etc. In the present invention, in order to suppress the formation of by-products, it is preferable to add the raw material 1 in two or more portions or to add a certain amount intermittently or continuously by dropping. In this case, the raw material 1 is added to the raw material 2 so that the amount of the acid halide compound represented by the general formula (5) contained in the raw material 1 (addition amount per minute) is 0.0027 mol / min or more, preferably 0.0035 mol / min or more, and particularly preferably 0.0069 mol / min or more, per 1 mol of sulfamide contained in the raw material 2. By setting the addition amount to 0.0027 mol / min or more, the amount of the acid halide compound represented by the general formula (5) in the reaction liquid in which the raw materials 1 and 2 are mixed can be controlled to an appropriate range, and it is considered that the formation of by-products can be suppressed. In particular, it is considered that the formation of the naphthalene compound represented by formula (c) can be suppressed. In this case, the time for adding reaction raw material 1 to reaction raw material 2 can be appropriately selected depending on the amount of reaction raw material 1 to be added, but is usually 5 minutes or more, preferably 10 minutes or more. If the amount of addition is less than 0.0027 mol / min, the amount of by-products may increase, and if the addition time is too short, a large amount of gas produced as a by-product from the reaction between reaction materials 1 and 2 may be generated suddenly. (Temperature of mixture) The temperature of the mixed liquid obtained by mixing the reaction raw materials 1 and 2 may vary depending on the organic solvent and catalyst used, etc., but the lower limit is usually 10°C or higher, preferably 15°C or higher, and particularly preferably 20°C or higher, from the viewpoints of quality, reactivity, cost, etc., and the upper limit is usually 100°C or lower, preferably 95°C or lower, and particularly preferably 90°C or lower, from the viewpoints of quality, reactivity, cost, etc. If the temperature of the mixture obtained by mixing the reaction raw materials 1 and 2 is lower than 15° C., the mixing may be insufficient, resulting in a decrease in reaction efficiency, and if it is higher than 90° C., the production of by-products may increase. In particular, if the temperature of the mixture is high, the compound represented by formula (5) reacts with the reaction product, and impurities such as the compound represented by formula (c) are likely to be produced, which may decrease the yield and quality of the 2-naphthylacetonitrile represented by formula (1).

[0080] [ka]

[0081] <Post-processing> The reaction solution containing 2-naphthylacetonitrile obtained in the step 2 may be subjected to treatment such as neutralization, liquid separation, filtration, etc., or the target 2-naphthylacetonitrile may be isolated by an isolation means such as concentration, crystallization with an organic solvent such as toluene, heptane, etc. In addition, the nitrile compound can be precipitated as crystals by adding a poor solvent such as water to the reaction solution containing the target 2-naphthylacetonitrile. For example, the resulting reaction liquid is cooled, an organic solvent such as toluene is added, the organic layer is washed with water and a base, the organic layer obtained after washing is concentrated, an organic solvent such as methanol is added to the concentrated residue to replace the solvent, the mixture is cooled, and the precipitated 2-naphthylacetonitrile is recovered by filtration. The resulting wet crystals are dried to obtain 2-naphthylacetonitrile as a solid. In addition, the 2-naphthylacetonitrile obtained in the present invention is of high quality, preferably having a purity (HPLC) of 98 area % or more, particularly preferably 99 area % or more, and may be further purified by known purification means such as recrystallization, column chromatography, and activated carbon treatment, if necessary.

[0082] In addition, each compound in the present invention may form a solvate such as a hydrate or an organic solvate, and the form is not particularly limited as long as it does not inhibit the reaction.

[0083] In the production method of the present invention, the steps 1 and 2 are particularly preferably the following steps.

[0084] Step 1: A step of reacting 2'-acetonaphthone, sulfur and morpholine, followed by hydrolysis to obtain 2-naphthylacetic acid.

[0085] [ka]

[0086] Step 2: A step of mixing a reaction raw material 1, which is a mixture of 2-naphthylacetic acid, thionyl chloride, toluene, and a catalyst as required, with a reaction raw material 2, which is a mixture of sulfamide and sulfolane, at 15°C to 90°C, and then heating and reacting at 80°C to 180°C to obtain 2-naphthylacetonitrile, or a step of adding the reaction raw material 1 to the reaction raw material 2 and reacting at 80°C to 180°C to obtain 2-naphthylacetonitrile, in which the reaction raw material 1 is added to the reaction raw material 2 so that the amount of the acid chloride contained in the reaction raw material 1 is 0.0027 mol / min or more per 1 mol of sulfamide contained in the reaction raw material 2. By this step 2, it is possible to suppress the production of the naphthalene compounds (by-products) explained in the section "High-purity 2-naphthylacetonitrile of the present invention", particularly the naphthalene compound represented by formula (c).

[0087] [ka] EXAMPLES

[0088] The present invention will be described in more detail below by way of examples, but the present invention is not limited to these examples. In the following Examples and Comparative Examples, commercially available 2'-acetonaphthone was used. The purity of the obtained compounds was measured by HPLC under the following analytical conditions.

[0089] (HPLC analysis conditions) Analytical equipment: Agilent HPLC (1200 series) Column: Zorbax Eclipse Plus Phenyl-Hexyl, 5 μm, 250 mm × 4.6 mm Mobile phase A: 0.1% by volume trifluoroacetic acid aqueous solution Mobile phase B: Acetonitrile Gradient: 0 min (B: 30%) - 15 min (B: 60%) - 20 min (B: 95%) - 30 min (B: 95%) Flow rate: 1.0 mL / min Injection volume: 5 μL Detection wavelength: 280 nm Column temperature: 40℃

[0090] Example 1 (1) Synthesis of 2-naphthylacetic acid

[0091] [ka]

[0092] 24 kg of 2'-acetonaphthone, 5.65 kg of sulfur (1.25 times by mole relative to 2'-acetonaphthone), 2.68 kg of paratoluenesulfonic acid monohydrate (0.1 times by mole relative to 2'-acetonaphthone), and 36.9 kg of morpholine (3 times by mole relative to 2'-acetonaphthone) were placed in a nitrogen-substituted reaction vessel, stirred, and reacted for 3 hours at 115°C to 120°C. The production of a thioamide was confirmed by HPLC. After the reaction liquid was cooled to 70-80°C, a 20% by weight aqueous solution of sodium hydroxide (a mixture of 16.9 kg of sodium hydroxide and 67.7 kg of water; 5 moles of sodium hydroxide per mole of 2'-acetonaphthone) was added, followed by the addition of 43.2 kg of water. The mixture was then heated and reacted at 90-105°C for 4 hours (hydrolysis). The reaction solution obtained was cooled to 65°C to 75°C, 24 kg of water and 83.2 kg of toluene were added, and the mixture was stirred at 65°C to 75°C, allowed to stand, and the upper layer obtained was discarded (removal of unreacted sulfur). The remaining lower layer (206.35 kg) was added to a mixture of 208.05 kg of toluene and 80.8 kg of hydrochloric acid with a concentration of 35% by weight. Furthermore, 2.4 kg of water was added to the reaction vessel containing the lower layer to wash it, and the liquid obtained after washing was also added to the mixture. The mixture containing the reaction solution obtained in this manner was stirred at 65°C to 75°C, allowed to stand (extraction of 2-naphthylacetic acid), and the lower layer obtained was discarded. 121.0 kg of water was added to the remaining upper layer, stirred at 65°C to 75°C, allowed to stand, and the lower layer was discarded. Furthermore, 121 kg of water was added to the remaining upper layer, stirred at 65°C to 75°C, allowed to stand, and the lower layer was discarded. The remaining upper layer was concentrated and then cooled to 10°C or less. The precipitated crystals of 2-naphthylacetic acid were collected by centrifugation and washed with 20.8 kg of toluene to obtain wet crystals. The obtained wet crystals were dried under reduced pressure in an atmosphere of 60°C to obtain 19.70 kg of 2-naphthylacetic acid. 1 H-NMR(400MHz, CDCl3)δ3.80 (2H, s), 7.40 (1H, dd, J=8.4, 3.0Hz), 7.43-7.49(2H, m), 7.73 (1H, s), 7.78-7.82 (3H, m)

[0093] (2) Synthesis of 2-naphthylacetonitrile

[0094] [ka]

[0095] Into a reaction vessel purged with nitrogen, 18.7 kg of 2-naphthylacetic acid obtained in (1) above, 40.55 kg of toluene, and 73.08 g of N,N-dimethylformamide were added. Furthermore, the equipment used in the above addition was washed with 16.2 kg of toluene, and the liquid obtained after washing was also added to the reaction vessel. 12.5 kg of thionyl chloride (1.05 times by mole relative to 2-naphthylacetic acid) was added to the obtained solution, and the reaction was carried out at 35°C to 45°C for 5 hours. After cooling to 20°C to 30°C, it was filtered. The obtained filtrate and the washing liquid obtained by washing the filtration residue with 8.15 kg of toluene were mixed, and 23.6 kg of sulfolane (1 volume times relative to 2-naphthylacetic acid) was added thereto, followed by concentration under reduced pressure to prepare an acid chloride solution. Into another reaction vessel purged with nitrogen, 11.6 kg of sulfamide (1.2 molar equivalent to 2-naphthylacetic acid), 58.9 kg of sulfolane (2.5 volume equivalent to 2-naphthylacetic acid), and 18.7 kg of inorganic additives were placed and stirred, and then the temperature was raised to 95°C to 105°C to prepare a sulfamide solution. The acid chloride solution was added dropwise to the sulfamide solution over 2 hours at 95° C. to 105° C. Furthermore, the reaction vessel containing the acid chloride solution was washed with 1.62 kg of toluene, and the liquid obtained after washing was also added to the reaction vessel, followed by reaction at 95° C. to 105° C. for 7 hours. The reaction solution obtained was cooled to 25°C, 65 kg of toluene and 74.8 kg of water were added, and the mixture was stirred at 20°C to 30°C, then allowed to stand, and the lower layer was discarded. 35.5 kg of water and 5.61 kg of potassium carbonate were added to the remaining upper layer, and the equipment used in the above reaction was washed with 15 kg of water, and the liquid obtained after washing was also added to the mixture containing the above upper layer. The mixture obtained was stirred at 20°C to 30°C, then allowed to stand, and the lower layer was discarded. 37.4 kg of water was added to the remaining upper layer, and the mixture was stirred at 20°C to 30°C, then allowed to stand, and the lower layer was discarded. The remaining upper layer was concentrated, and 104 kg of methanol was added, and the mixture was further concentrated. 44.4 kg of methanol was added to the obtained concentrated liquid, and the mixture was concentrated. 0.374 kg of activated carbon and 45.1 kg of methanol were added to the obtained concentrated liquid at 35°C, and the mixture was stirred and filtered. The filtration residue was washed with 14.95 kg of methanol, and the filtrate and the liquid after washing were mixed. The resulting mixed solution was kept at 30°C to 40°C for about 90 minutes, then cooled, and 74.8 kg of water (4 volumes of 2-naphthylacetic acid) was added at a temperature of about 10°C, and stirred for 4 hours. The precipitated crystals were collected by centrifugation, and the collected wet crystals were washed with an aqueous methanol solution (a mixed solution of 14.8 kg of methanol and 18.7 kg of water). The obtained wet crystals were dried under reduced pressure in an atmosphere of 60°C, and 15.2 kg of 2-naphthylacetonitrile crystals (purity 99.50 area%) were obtained. 1 H-NMR(400MHz, CDCl3)δ3.92 (2H, s), 7.37-7.40 (1H, m), 7.49-7.54 (2H, m), 7.83-7.85 (4H, m)

[0096] The HPLC analysis results of the obtained 2-naphthylacetonitrile are shown in Table 3 and Figure 1. In Table 3, RRT is the relative retention time when the retention time of 2-naphthylacetonitrile is set to 1.00.

[0097] [Table 3]

[0098] Moreover, the HPLC analysis results showed that the compounds of formulae (e) to (j) were not detected in the obtained 2-naphthylacetonitrile. In addition, the compounds of the formulas (a) to (d) 1 The H-NMR measurement results are as follows:

[0099] Compound of formula (a)

[0100] [ka]

[0101] 1 H-NMR(400MHz, CDCl3)δ = 3.71 (s, 3H), 3.79 (s, 2H), 7.40-7.47 (m, 3H), 7.73 (s, 1H), 7.79-7.83(m, 3H)

[0102] Compound of formula (b)

[0103]

Chem.

[0104] LC / MS 215 (m / z, Pos) 1 1H-NMR (400 MHz, CDCl3) δ = 1.26 (t, J = 7.2 Hz, 3H), 3.78 (s, 2H), 4.17 (q, J = 7.2 Hz, 2H), 7.41 - 7.49 (m, 3H), 7.74 (s, 1H), 7.79 - 7.82 (m, 3H)

[0105] Compound of formula (c)

[0106]

Chem.

[0107] LC / MS 354 (m / z, Pos) 1 1H-NMR (400 MHz, dmso-d6) δ = 4.03 (s, 4H), 7.41 (dd, J = 8.4, 1.6 Hz, 2H), 7.48 - 7.50 (m, 4H), 7.75 (s, 2H), 7.82 - 7.90 (m, 6H), 11.12 (s, 1H)

[0108] Compound of formula (d)

[0109]

Chem.

[0110] LC / MS 503 (m / z, Pos) 1H-NMR(400MHz, CDCl3)δ = 1.27(s,9H),3.54(s,2H),3.59(s,2H),7.04(d,J = 8.8Hz,1H),7.11(d,J = 2.0Hz,1H),7.21(dd,J = 8.4,2.4Hz,1H),7.29-7.34(m,2H),7.42-7.49(m,4H),7.59(s,1H),7.63(s,1H),7.76-7.79(m,6H)

[0111] Example 2 In a nitrogen-substituted reaction vessel, 75.02 g of 2-naphthylacetic acid synthesized according to the method of Example 1(1), 263 mL of toluene (3.5 times by volume relative to 2-naphthylacetic acid), and 0.29 g of N,N-dimethylformamide (0.01 times by mole relative to 2-naphthylacetic acid) were added, and the temperature was raised to 35°C to 45°C, and 50.3 g of thionyl chloride (1.05 times by mole relative to 2-naphthylacetic acid) was added. After reacting for 3 hours, the reaction liquid was concentrated to prepare reaction material 1 containing 2-naphthylacetic acid chloride. Into another reaction vessel purged with nitrogen, 46.49g of sulfamide (1.2 molar times relative to 2-naphthylacetic acid), 74.99g of inorganic additive (1 weight times relative to 2-naphthylacetic acid), and 263mL of sulfolane (3.5 volume times relative to 2-naphthylacetic acid) were added and heated (preparation of reaction material 2). At 95°C to 105°C, reaction material 1 containing 2-naphthylacetic acid chloride was added dropwise to reaction material 2 over 18 minutes, and then the equipment used in the preparation of reaction material 1 was washed with 7.5mL of toluene (0.1 volume times relative to 2-naphthylacetic acid), and the solution obtained was further added to reaction material 2 and reacted at 95°C to 105°C for 4 hours. The reaction solution was analyzed by HPLC, and after confirming the disappearance of the raw materials, it was cooled to 20°C to 30°C, 300mL of water (4 times by volume relative to 2-naphthylacetic acid) and 300mL of toluene (4 times by volume relative to 2-naphthylacetic acid) were added and stirred, and the aqueous layer was discarded. The remaining organic layer was washed with 225.08g of 10% potassium carbonate aqueous solution (3 times by weight relative to 2-naphthylacetic acid) and 150mL of water (2 times by volume relative to 2-naphthylacetic acid). The obtained organic layer was concentrated, and 525 mL of methanol (7 times by volume relative to 2-naphthylacetic acid) was added to the concentrated residue, and the mixture was concentrated again. Further, methanol was added to the obtained concentrated residue to adjust the liquid volume to 525 mL, and then 1.52 g of activated carbon (0.02 times by weight relative to 2-naphthylacetic acid) was added, stirred at 50°C to 60°C, and filtered. The obtained filtration residue was washed with 75 mL of methanol (1 time by volume relative to 2-naphthylacetic acid). The filtrate was cooled to 5°C to 15°C, and then 300 mL of water (four volumes of 2-naphthylacetic acid) was added and stirred. The precipitated 2-naphthylacetonitrile was collected by filtration, and the resulting wet crystals were dried to obtain 60.38 g of 2-naphthylacetonitrile (purity 99.85 area%) as a solid. The reaction solution after 4 hours of reaction and the HPLC analysis results of the resulting 2-naphthylacetonitrile are shown in Table 4.

[0112] [Table 4]

[0113] Moreover, the results of HPLC analysis showed that the compounds of formulae (d) to (j) were not detected in the obtained crystals of 2-naphthylacetonitrile.

[0114] Example 3

[0115] [ka]

[0116] 25g of 2-naphthylacetic acid synthesized according to the method of Example 1(1), 75.88g of toluene (3.5 times by volume relative to 2-naphthylacetic acid), and 0.0982g of N,N-dimethylformamide (0.01 times by mole relative to 2-naphthylacetic acid) were added to a reaction vessel purged with nitrogen. 16.77g of thionyl chloride (1.05 times by mole relative to 2-naphthylacetic acid) was added dropwise to the resulting solution, and the mixture was reacted at 43°C to 45°C for 3 hours. After that, 10.88g of toluene (0.5 times by volume relative to 2-naphthylacetic acid) and 31.53g of sulfolane (1 time by volume relative to 2-naphthylacetic acid) were added, and the mixture was concentrated under reduced pressure to prepare a reaction material 1 containing 2-naphthylacetic acid chloride. Into another reaction vessel purged with nitrogen, 15.5g of sulfamide (1.2 molar equivalent to 2-naphthylacetic acid), 78.78g of sulfolane (2.5 volume equivalent to 2-naphthylacetic acid), and 25.01g of inorganic additives were added, stirred, and then heated to 75°C to 85°C (preparation of reaction raw material 2). This reaction raw material 2 was in a slurry state, not a solution. At 75°C to 85°C, reaction material 1 containing 2-naphthylacetic acid chloride was added dropwise to reaction material 2 over 10 hours, and the temperature was then increased to 100°C over 2 hours, and the reaction was carried out for 5 hours. The obtained reaction liquid was cooled to 55°C to 65°C, and 86.7g of toluene (4 times by volume relative to 2-naphthylacetic acid) and 100.05g of water (4 times by volume relative to 2-naphthylacetic acid) were added and stirred, then allowed to stand, and the lower layer was discarded. 75.01g of 5% by weight aqueous sodium hydrogen carbonate solution (3 times by weight relative to 2-naphthylacetic acid) was added to the remaining upper layer, and the mixture was stirred at 55°C to 65°C, then allowed to stand, and the lower layer was discarded. 50.01g of water (2 times by weight relative to 2-naphthylacetic acid) was added to the remaining upper layer, and the mixture was stirred at 55°C to 65°C, then allowed to stand, and the lower layer was discarded. The remaining upper layer was concentrated, and 138.44g of methanol (7 times by volume relative to 2-naphthylacetic acid) was added to the concentrated residue, and the mixture was further concentrated. The concentrated residue was concentrated by adding 59.34 g of methanol (3 times by volume relative to 2-naphthylacetic acid), and then 39.55 g of methanol (2 times by volume relative to 2-naphthylacetic acid) and 0.5 g of activated carbon (0.02 times by weight relative to 2-naphthylacetic acid) were added to the concentrated residue, followed by filtration. The filtrate was mixed with a washing liquid obtained by washing the filtration residue with 19.78 g of methanol (1 time by volume relative to 2-naphthylacetic acid), to obtain a 2-naphthylacetonitrile solution. The obtained 2-naphthylacetonitrile solution was heated to 40°C to 50°C, 0.1259g of water (0.005 volume times relative to 2-naphthylacetic acid) and 0.0248g of potassium carbonate (0.001 weight times relative to 2-naphthylacetic acid) were added and stirred for 1 hour, and then 100g of water (4 volume times relative to 2-naphthylacetic acid) was added dropwise over 1 hour. Then, the mixture was cooled and stirred at a temperature of about 10°C for 1 hour. The precipitated crystals were filtered, and the collected wet crystals were washed twice with an aqueous methanol solution (a mixed solution of 27.71g of methanol and 15.03g of water). The obtained wet crystals were dried under reduced pressure at an atmosphere of 60°C, and 19.09g of 2-naphthylacetonitrile was obtained as crystals (yield 85%, purity 99.87 area%).

[0117] The HPLC analysis results of the obtained 2-naphthylacetonitrile are shown in Table 5 and FIG.

[0118] [Table 5]

[0119] In addition, the HPLC analysis results showed that the compounds of formulae (b) and (e) to (j) were not detected in the obtained crystals of 2-naphthylacetonitrile. According to this example, 2-naphthylacetonitrile was obtained that contained less impurities, such as the compounds of formulae (a) and (c), than in Examples 1 and 2. In particular, the 2-naphthylacetonitrile obtained in this example does not contain the compound of formula (c), and is useful as a raw material or intermediate for the synthesis of pharmaceuticals. In this manner, it is found that by mixing the reaction raw material 1 containing 2-naphthylacetic acid chloride and the reaction raw material 2 containing sulfamide at a relatively low temperature and then reacting them at elevated temperature, high-purity 2-naphthylacetonitrile with a low impurity content can be obtained.

[0120] Example 4 In a nitrogen-substituted reaction vessel, 10.03 g of 2-naphthylacetic acid synthesized according to the method of Example 1 (1), 35 mL of toluene (3.5 times by volume relative to 2-naphthylacetic acid), and 42 μL of N,N-dimethylformamide (0.01 times by mole relative to 2-naphthylacetic acid) were added, and the temperature was raised, and 6.72 g of thionyl chloride (1.05 times by mole relative to 2-naphthylacetic acid) was added at 35°C to 45°C. After reacting for 2 hours, the mixture was cooled and filtered at room temperature, and the filtration residue was washed with 5 mL of toluene. 10 mL of sulfolane (1 time by volume relative to 2-naphthylacetic acid) was added to the obtained filtrate and washed liquid, and then the mixture was concentrated to prepare a reaction material 1 containing 2-naphthylacetic acid chloride. In another reaction vessel purged with nitrogen, 6.19 g of sulfamide (1.2 molar times relative to 2-naphthylacetic acid), 10.01 g of inorganic additive (1.0 weight times relative to 2-naphthylacetic acid), and 25 mL of sulfolane (2.5 volume times relative to 2-naphthylacetic acid) were added and heated (preparation of reaction material 2). At 95°C to 105°C, reaction material 1 containing 2-naphthylacetic acid chloride was added dropwise to reaction material 2 over 1 hour, and then a solution obtained by washing the equipment used in the preparation of reaction material 1 with 1 mL of toluene (0.1 volume times relative to 2-naphthylacetic acid) was further added, and the reaction was carried out at 95°C to 105°C for 4 hours. The reaction solution was analyzed by HPLC and found to contain 96.27 area % of 2-naphthylacetonitrile and 0.39 area % of the compound of formula (c). The reaction solution was cooled to 25°C, 40mL of water (4 times by volume relative to 2-naphthylacetic acid) and 40mL of toluene (4 times by volume relative to 2-naphthylacetic acid) were added and stirred, and the lower layer was discarded. The remaining organic layer was washed with 30.32g of 10% by weight potassium carbonate aqueous solution (3 times by weight relative to 2-naphthylacetic acid) and 20mL of water (2 times by volume relative to 2-naphthylacetic acid). The organic layer obtained was concentrated, and 70 mL of methanol (7 times by volume relative to 2-naphthylacetic acid) was added to the concentrated residue, followed by concentrating again. Further, methanol was added to the concentrated residue obtained to adjust the liquid volume to 70 mL, and 0.2 g of activated carbon (0.02 times by weight relative to 2-naphthylacetic acid) was added, and the mixture was stirred at 40°C to 50°C, filtered, and the filtration residue was washed with 10 mL of methanol (1 time by volume relative to 2-naphthylacetic acid). The obtained filtrate was cooled to 5°C to 15°C, and then 40 mL of water (four volumes of 2-naphthylacetic acid) was added and stirred. The precipitated 2-naphthylacetonitrile was collected by filtration, and the obtained wet crystals were dried to obtain 8.11 g of 2-naphthylacetonitrile (purity 99.30 area %) as a solid. The reaction solution after 4 hours of reaction and the HPLC analysis results of the resulting 2-naphthylacetonitrile are shown in Table 6.

[0121] [Table 6]

[0122] Moreover, the results of HPLC analysis showed that the compounds of formulae (d) to (j) were not detected in the obtained crystals of 2-naphthylacetonitrile.

[0123] Example 5 The reaction was carried out in the same manner as in Example 4, except that the time for dropping the reaction material 1 was changed from 1 hour to 8 minutes. The reaction liquid obtained by reacting the reaction materials 1 and 2 for 4 hours was measured by HPLC and found to contain 95.94 area % of 2-naphthylacetonitrile and 0.30 area % of the compound of formula (c).

[0124] Example 6 The reaction was carried out in the same manner as in Example 4, except that the time for dropping the reaction raw material 1 was changed from 1 hour to 4 hours. The reaction liquid obtained by reacting the reaction materials 1 and 2 for 4 hours was measured by HPLC and found to contain 96.37 area % of 2-naphthylacetonitrile and 0.70 area % of the compound of formula (c).

[0125] Comparative Example 1 2-Naphthylacetonitrile was synthesized in the same manner as in Example 4, except that the time for dropping the reaction material 1 was changed from 1 hour to 10 hours. The reaction liquid obtained by reacting the reaction materials 1 and 2 for 4 hours was measured by HPLC and found to contain 92.75 area % of 2-naphthylacetonitrile and 1.16 area % of the compound of formula (c). Furthermore, HPLC analysis of the resulting 2-naphthylacetonitrile revealed that the content of 2-naphthylacetonitrile was 97.44 area %, and the content of the compound of formula (c) was 0.47 area %.

[0126] Table 7 shows the dropwise addition time and amount of the reaction raw material 1, and the contents of 2-naphthylacetonitrile and the compound of formula (c) in the reaction liquid obtained after 4 hours of reaction. In Table 7, the amount of reaction raw material 1 added means the amount of acid chloride compound contained in reaction raw material 1 added per 1 mol of sulfamide contained in reaction raw material 2 (mol / min).

[0127] [Table 7]

[0128] As is clear from Table 7, the greater the amount (mol / min) of the acid chloride compound contained in the reaction raw material 1, the smaller the amount of the compound of formula (c) produced. However, if the amount (mol / min) of the acid chloride compound contained in the reaction raw material 1 is too large, there is a risk of a large amount of hydrochloric acid gas being generated as a by-product. Therefore, in the case of industrial mass production, it is necessary to take safety precautions, such as by installing a treatment device. [Industrial Applicability]

[0129] According to the present invention, it is possible to provide high-purity 2-naphthylacetonitrile with few impurities, which is useful as a raw material or intermediate for synthesizing various pharmaceuticals, agricultural chemicals, and chemical products, particularly as a raw material or intermediate for synthesizing pharmaceuticals. It is also possible to provide a method for producing high-purity 2-naphthylacetonitrile that is safe, highly efficient, and can be produced industrially and in large quantities at low cost. Furthermore, by using the 2-naphthylacetonitrile of the present invention, pharmaceuticals such as (1R,5S)-1-(naphthalen-2-yl)-3-azabicyclo[3.1.0]hexane can be produced industrially and in large quantities at low cost.

[0130] This application is based on patent application No. 2019-196782 filed in Japan (filing date: October 29, 2019), the contents of which are incorporated herein by reference in their entirety.

Claims

1. A compound represented by the following general formula (5) obtained by reacting 2-naphthylacetic acid with a halogenating agent. 【Chemistry 1】 (In general formula (5), X represents a halogen atom.) and a reaction raw material 2 containing sulfamide at 10°C to 100°C, and then the mixture is heated to 85°C to 120°C to obtain 2-naphthylacetonitrile.

2. A method for producing high-purity 2-naphthylacetonitrile as described in claim 1, characterized in that reaction raw material 1 is added to reaction raw material 2 at 10°C to 100°C, and the temperature is raised to 85°C to 120°C to obtain 2-naphthylacetonitrile.

3. A method for producing high-purity 2-naphthylacetonitrile as described in claim 1 or 2, characterized in that the amount of the sulfamide is 1 mol to 5 mol per 1 mol of the 2-naphthylacetic acid.

4. A compound represented by the general formula (5) with respect to 1 mol of the sulfamide. 【Chemistry 2】 The method for producing high purity 2-naphthylacetonitrile according to any one of claims 1 to 3, characterized in that the reaction material 1 is added to the reaction material 2 so that the amount of the acid halide represented by the following formula is 0.0027 mol / min or more.

Images