470 results about "Decarboxylation" patented technology

The invention relates to the technical field of microorganisms, and particularly discloses a recombinant microorganism and application thereof in fermentation production of decarboxylated carnosine. Compared with an original strain, the recombinant microorganism disclosed by the invention has the advantages that the expression of the mdtK gene is enhanced; the starting strain is escherichia coli capable of producing decarboxylated carnosine. When the recombinant microorganism is used for fermentation production, the yield of the decarboxylated carnosine can be increased, L-histidine, histamine or beta-alanine and other precursors do not need to be added in the production process, and an effective novel method is provided for industrial production of the decarboxylated carnosine.

The present invention relates to the fields of medicine and cosmetology, and discloses a cell active peptide composition that promotes the regeneration of multi-type collagen structural proteins, its preparation method, and its application in medicine and cosmetology. The composition uses raw materials such as tripeptide-10 citrulline, hexapeptide-9, hydrolyzed sodium hyaluronate, γ-aminobutyric acid, decarboxylated carnosine hydrochloride, acetyl tetrapeptide-3, acetyl tetrapeptide-11, palmitoyl dipeptide-7, and palmitoyl pentapeptide-4. The composition can promote the coordinated expression of skin type I, type III, type IV, type VII, type XVII collagen, fibronectin, elastin, and glycosaminoglycans; prevent collagen cross-linking, maintain triple helix structure, and inhibit collagen degradation. Applied to dermatology and cosmetology, it can accelerate the regeneration of structural proteins such as skin collagen, repair skin damage, reduce wrinkles such as crow's feet, tear groove lines, nasolabial folds, and under-eye lines, solve the skin aging problem caused by the loss of structural proteins such as collagen, and improve skin elasticity and firmness.

The invention belongs to the field of organic synthetic chemistry, and relates to a preparation method of melatonin and meerythrine indole derivatives and compounds. Specifically, the indole derivative is efficiently synthesized by taking arylamine and carboxylic acid as raw materials through a one-pot two-step reaction in the presence of catalysis of ferric chloride hexahydrate (FeCl3. 6H2O), a ligand, a diazotization reagent, an additive and a solvent under the conditions of visible light irradiation, inert atmosphere and room temperature. According to the method, visible light induced iron-based LMCT catalysis and iron lewis acid catalysis functions are integrated, and efficient integration of diazotization, decarboxylation, free radical coupling and cyclization reaction is achieved. The method has the advantages that raw materials are cheap and easy to obtain, reaction conditions are mild, substrate applicability is wide, functional group compatibility is good, operation is easy, convenient and safe, and environment friendliness is achieved, gram-level scale preparation can be achieved, and a green and efficient synthesis path is provided for indole compounds with biological activity such as melatonin and meerythrine.

The invention discloses application of laccase as a catalyst in catalytic synthesis of allantoin. According to the invention, laccase from thermophilus is used as an enzyme catalyst, uric acid is oxidized, hydrolyzed and decarboxylated to synthesize allantoin, and efficient biosynthesis of allantoin is realized under mild conditions; wherein the amino acid sequence of the laccase derived from the thermophilic fungi is as shown in SEQ ID NO. 1. The invention provides an efficient, environment-friendly and low-cost biosynthesis approach for biosynthesis of allantoin, and has industrial application prospects in biosynthesis of allantoin.

The invention belongs to the technical field of separation of drug intermediates, and particularly relates to a control method for a process impurity 2-ethyl valeric acid (EP-B) in preparation of valproic acid or sodium valproate by a diethyl malonate method. According to the method disclosed by the invention, the content of 2-ethyl-2-propylmalonic acid process impurities in dipropylmalonic acid is controlled, so that the content of 2-ethylvaleric acid (EP-B) which is a process impurity in valproic acid or sodium valproate is accurately controlled; adding a polar solvent into the dipropylmalonic acid crude product, heating, pulping for a certain time, cooling, filtering and drying to obtain a high-purity dipropylmalonic acid refined product; high-purity valproic acid (RRT is equal to 1.00) is prepared through decarboxylation of the dipropyl malonic acid fine product, and the purity is 99.779%; 0.020% of 2-ethyl valeric acid (RRT is equal to 0.90); and valeric acid (RRT = 0.77), 0.039%. The valproic acid product quality meets the requirements of European Pharmacopoeia. According to the method, the problems of quality control and process evaluation of valproic acid or sodium valproate prepared by a diethyl malonate method are solved.

The invention relates to the technical field of pesticides, and discloses a fluopyram compound and a preparation method thereof. The preparation method of the fluopyram compound comprises the following steps: 1) in the presence of a first organic solvent and first alkali, carrying out nucleophilic substitution reaction on a compound with a structure as shown in a formula (1) and a compound with a structure as shown in a formula (2); 2) carrying out a decarboxylation reaction on the nucleophilic substitution reaction product obtained in the step 1) in the presence of a first solvent and a first acid; 3) in the presence of a second solvent and a second acid, the decarboxylation reaction product obtained in the step 2) is subjected to a decyanation reaction to obtain the fluopyram compound, in the formula (1), X represents halogen, and R1 represents-COOC1-6 alkyl; in formula (2), R2 represents an alkyl group having 1-6 carbon atoms. According to the preparation method of the fluopyram compound, the yield is higher, and the operation is more convenient. # imgabs 0 # formula (1) # imgabs 1 # formula (2).

A method for providing a cargo to a C-terminal end of a peptide comprises a first stage and a second stage, wherein the first stage comprises reacting the C-terminal end of the peptide with a first reactant in the presence of a first catalyst and first radiation to provide a first intermediate, wherein the first catalyst is configured to decarboxylate the C-terminal end of the peptide in the presence of the first radiation; and wherein the second stage comprises exposing the first intermediate to a second reactant.

Various aspects of this disclosure relate to methods to lower the activation energy of the cannabinoid decarboxylation reaction by performing the decarboxylation reaction in the gas phase. In some specific embodiments, the method relates to the decarboxylation of a cannabinoid performed in a short-path distillation apparatus or a thin-film distillation apparatus.

The invention relates to a method for preparing high-molecular-weight polyethylene furandicarboxylate by a one-step method, and belongs to the technical field of bio-based polyester materials. The method comprises the following steps: weighing raw materials including 2, 5-furandicarboxylic acid, ethylene glycol, an end group regulator, a protective agent, a decarboxylation inhibitor and a catalyst, mixing and adding into a reaction container, introducing nitrogen, maintaining the pressure of the nitrogen in the reaction container to be 50-150 kPa, carrying out esterification reaction, heating and vacuumizing until the pressure is less than or equal to 50 Pa after the esterification reaction is completed, and carrying out polycondensation reaction to obtain the 2, 5-furandicarboxylic acid. And carrying out extrusion and drying so as to obtain the high-molecular-weight polyethylene furandicarboxylate, wherein the high-molecular-weight polyethylene furandicarboxylate is obtained. According to the method, the FDCA conversion rate is larger than or equal to 98%, the number-average molecular weight of the obtained product is larger than or equal to 32 kg / mol, no heavy metal residues exist, and the method is suitable for large-scale production of high-end bio-based packaging materials.

The invention discloses a method for synthesizing thioamide through photocatalysis. According to the method, sulfur powder, ketonic acid and amine are taken as starting raw materials, and the thioamide compound is synthesized in a green and efficient manner through dehydration condensation, photooxidation reduction decarboxylation and coupling sulfur insertion at room temperature under blue light irradiation. The method designed by the invention is novel and efficient, the raw materials are green and odorless, the synthesis method is simple, the conditions are mild, the yield is higher, the substrate application range is wide, and the method has very strong popularization potential.

The invention belongs to the technical field of separation of drug intermediates, and particularly relates to a method for preparing a high-purity dipropylmalonic acid refined product by adding a polar solvent into a dipropylmalonic acid crude product, heating, pulping for a certain time, cooling, filtering and drying. Decarboxylating the refined dipropylmalonic acid product to obtain high-purity valproic acid; distilling the filtrate to recover the polar solvent to obtain 2-methyl-2-propylmalonic acid, and carrying out decarboxylation on the 2-methyl-2-propylmalonic acid to obtain 2-methylpentanoic acid; 2-methylvaleric acid is used as a perfume additive. According to the method disclosed by the invention, the process impurity 2-methyl-2-propylmalonic acid in dipropylmalonic acid is separated, and the process impurity 2-methylvaleric acid (EP-L) in valproic acid or sodium valproate is precisely separated; the quality of the valproic acid product prepared by the method disclosed by the invention meets the requirements of European Pharmacopoeia EP-11 (2023). According to the invention, the problems of quality control and process evaluation of valproic acid or sodium valproate prepared by a dimethyl malonate method are solved.

The invention belongs to the field of cosmetics, and particularly discloses an ormosia henryi bark extract-containing composition capable of nourishing, repairing and brightening skin as well as a preparation method and application of the composition. The composition comprises an active component, a solubilizer, polyol, phospholipid and water, wherein the active ingredients comprise an ormosia henryi bark extract, acetylchitosamine, decarboxylated carnosine or salt thereof and a coast pine bark extract. Active ingredients in the composition are good in solubility in the composition, the composition is good in stability, good in skin permeability and good in AGEs inhibition effect, the four active ingredients including the ormosia henryi bark extract, the acetylchitosamine, the decarboxylated carnosine and the coast pine bark extract are in mutual synergistic interaction, and an excellent unexpected technical effect is achieved.

The invention discloses a mercury-resistant and mercury-removal Leclercia adcarboxsaca and an application thereof. The strain number of the Leclercia adecarboxyla disclosed by the invention is W13, and the preservation number of the Leclercia adecarboxyla is CGMCC (China General Microbiological Culture Collection Center) NO.34142. The strain disclosed by the invention is an efficient growth-promoting bacterial strain capable of resisting mercury, removing mercury and promoting growth, and particularly has a very strong effect on removing mercury by promoting mercury volatilization; in addition, the strain can be colonized in miscanthus sinensis, promote growth of miscanthus sinensis in a mercury-polluted environment, promote absorption of miscanthus sinensis to mercury in soil and promote volatilization of mercury in soil, so that the combination of Leclercia adcarboxamide and miscanthus sinensis can effectively repair mercury-polluted soil, and has a wide application prospect in treatment of mercury-polluted soil.

The invention provides a preparation method of an omariglitazone intermediate, which comprises the following steps: by taking p-halogenated benzaldehyde as a raw material, carrying out aldol condensation reaction, hydrolysis, decarboxylation, reduction, ring closing and the like to obtain an intermediate as shown in a formula 9, carrying out catalytic reaction, reduction reaction, ring closing and the like to obtain an intermediate as shown in a formula 13, and finally hydrolyzing to obtain a target product omariglitazone intermediate A. According to the invention, links of precious metal use and chiral resolution (key steps influencing cost and yield) in the prior art are avoided, and a method for synthesizing a single configuration through a chemical method is adopted, so that the yield is greatly improved, and the production cost is greatly reduced; meanwhile, a synthesis route is broken through, a target product is synthesized through cheap initial materials, and post-treatment is simpler and more controllable.

The present invention relates to a process for preparing aniline or an aniline conversion product, comprising the steps of (A) providing aminobenzoic acid; (B) decarboxylating the aminobenzoic acid in a reactor at a reaction temperature in the range from 170° C. to 350° C. to give aniline and carbon dioxide, wherein the decarboxylation is conducted at a reaction pressure at which the boiling point of aniline is reached or—preferably—exceeded, such that a first, liquid, phase possibly containing solid particles and a second, gaseous, phase form in the reactor, with a gaseous stream containing aniline and carbon dioxide being discharged from the reactor; and (C) condensing and optionally purifying the aniline present in the gaseous stream; and (D) optionally, converting the aniline obtained in (C) to an aniline conversion product.

The invention discloses a method for preparing a biological hydrocarbon compound by organic photocatalysis higher fatty acid decarboxylation, which comprises the following steps: adding higher fatty acid, a hydrogen atom transfer catalyst and an acridine photocatalyst / solid-phase acridine photocatalyst into a reaction solvent, stirring and reacting for 12-24 hours under the conditions of blue light irradiation and room temperature to obtain a reaction solution, filtering, washing and drying to obtain the biological hydrocarbon compound. And removing the reaction solvent of the obtained reaction solution under reduced pressure, and purifying by thin layer chromatography / column chromatography to obtain the long-chain alkane compound after decarboxylation of the higher fatty acid. The method is simple in step, mild in reaction condition and high in product yield, does not use any metal compound, and has the characteristics of high atom economy and environmental protection. And for unsaturated carboxylic acid, olefin configuration before and after decarboxylation is not influenced. When solid-phase acridine is used as a photocatalyst for reaction, the catalyst can be recycled through simple washing, filtering and recycling, excellent catalytic activity can still be kept after the catalyst is recycled for more than 10 times, and the reaction cost is further reduced.

The invention relates to a synthesis method of milobalin or acid salt thereof, and belongs to the technical field of medicine synthesis. In order to solve the problem that chiral resolution needs to be adopted in the prior art, the invention provides a synthesis method of miloabalin or an acid salt thereof, which comprises the following steps: under the action of an organic strong base, carrying out Michael addition reaction on a compound shown as a formula III and acetonitrile in a non-polar organic solvent at a low temperature of-50 DEG C or below to obtain an intermediate product; under the alkaline condition, the intermediate product is subjected to an oxidation reaction and a hydrolysis reaction under the action of an oxidizing agent, after the reaction is finished, an intermediate product is obtained through acidification, and the intermediate product is subjected to a high-temperature decarboxylation reaction in an aprotic solvent to obtain a compound of a formula VI; and carrying out Hofmann degradation reaction on the compound of formula VI to obtain the compound of formula I miloabalin or miloabalin acid salt. The method has the advantages of high stereoselectivity, no need of chiral resolution operation, avoidance of the problem of large material loss caused by resolution, high chiral purity and high yield.

The present invention relates to a decarboxylated carnosine derivative, a preparation method thereof and an application. The structural formula of the decarboxylated carnosine derivative of the present invention is shown in formula (I), wherein R is selected from: C5-C 21 alkyl group, C5-C 21 unsaturated hydrocarbon group. The decarboxylated carnosine derivative of the present invention has a more excellent anti-glycation effect compared with decarboxylated carnosine; meanwhile, it has good antioxidant effect; and, the decarboxylated carnosine derivative of the present invention has certain lipophilicity, is relatively easy to penetrate through the skin cutin layer, has good skin penetration performance, and has good stability at the same time. It can be used for preparing cosmetics with anti-glycation, antioxidant, anti-skin aging and other functions, and has important market value#imgabs0#(I).

The invention discloses a salicylic acid decarboxylase mutant and application of the salicylic acid decarboxylase mutant in degradation of salicylic acid. The mutant is obtained by carrying out site-specific modification on salicylic acid decarboxylase NahG, and specifically, valine at the 46th site, tyrosine at the 380th site and leucine at the 382nd site of an amino acid sequence shown in SEQ ID NO.2 are mutated into cysteine, phenylalanine and phenylalanine at the same time. The mutant shows remarkably improved catalytic efficiency, and salicylic acid can be efficiently and thoroughly decarboxylated and converted into catechol under mild conditions. The invention also provides a coding gene, a recombinant vector and an engineering bacterium of the mutant. The mutant not only can be used for efficient bioremediation of salicylic acid pollution, but also can effectively break through and accelerate a naphthalene catabolism pathway due to the characteristic of directionally generating catechol, and has important application value in the fields of environmental pollution abatement and biological catalysis.

The present invention relates to the field of microbial technology, and specifically discloses a recombinant microorganism and its application in the fermentation production of decarboxylated carnosine. The recombinant microorganism of the present invention has enhanced mdtK The starting strain is Escherichia coli capable of producing decarboxylated carnosine. Fermentation production using the recombinant microorganism of the present invention can increase the yield of decarboxylated carnosine without adding precursors such as L-histidine, histamine, or β-alanine during the production process, thereby providing an effective new method for the industrial production of decarboxylated carnosine.

The invention discloses a ZnTi-LDH modified UiO-66 nano composite material modified electrode rich in defects, a preparation method of the electrode and application of the electrode to detection of glyphosate pesticides. The preparation method comprises the following steps: firstly, treating UiO-66 by adopting a surface controlled decarboxylation defect technology to obtain defect-rich UiO-66, then preparing ZnTi-LDH on the surface of the UiO-66 in situ by adopting a hydrothermal method to obtain the ZnTi-LDH-coated D-UiO-66 heterostructure, and the structure can provide a large specific surface area and rich active sites, simultaneously contains Zr and Ti two metal types capable of complexing with organic phosphine molecules, and can be used for preparing a high-specific-surface-area catalyst. The adsorption and capture of the catalyst on an analyte are greatly improved, and the sensing analysis performance of a corresponding sensor on an organic phosphine pesticide is improved. An electrochemical sensing platform constructed on the basis of the ZnTi-LDH-coated D-UiO-66 nanocomposite modified electrode obtains a wide detection range (0.05-50 [mu] mol L1), a low detection limit of 0.19 [mu] mol / L (S / N = 3) and high sensitivity (1.220 [mu] A.[ mu] mol / L) when glyphosate is detected, and has good selectivity, reproducibility and stability.

The present invention discloses a pyruvate decarboxylase mutant with improved catalytic efficiency and its application. The present invention constructs a pyruvate decarboxylase mutant derived from Candida tropicalis for catalytic production of 4-hydroxyphenylacetaldehyde. The catalytic half-life (5.7 h) and TTN (24,600) of the mutant of the present invention are increased by 2.85 times and 2.07 times respectively compared with the control, and the mutant exhibits high decarboxylation activity. When the obtained mutant of the present invention uses 4-hydroxyphenylpyruvic acid as a substrate and reacts for 12 h at 25 °C and pH 6.5, the yield of 4-hydroxyphenylacetaldehyde can reach 5.08 g / L, and the molar conversion rate of the substrate reaches 67.28%. By adopting the method of the present invention, the production capacity of the unit catalyst and the reaction efficiency of the catalyst are improved, and the industrialization process of producing 4-hydroxyphenylacetaldehyde by the enzyme conversion method is accelerated.

The application relates to the technical field of catalysts and compound preparation, in particular to a metal-modified zeolite catalyst and a method for catalyzing lactone compounds to generate terminal olefins. ‑ SiO2; wherein the metal M is selected from any one of Ti, Cr, Mn, Co, Ni, Cu, Zn, Zr, Nb, W, Ta and Hf; in the provided metal-modified zeolite catalyst, metal atoms are arranged on the skeleton end points of a zeolite molecular sieve to form a monatomic catalyst; on one hand, the obtained catalyst has Lewis metal sites, can be beneficial to catalyzing lactone compounds to realize decarboxylation, and can ensure that the lactone compounds can be directly catalyzed to generate terminal olefins, and can be widely applied.

The invention discloses a preparation method of 3-quinuclidinone hydrochloride, which comprises the following steps: carrying out temperature control reaction on 4-picolinic acid and chloroacetic acid under alkaline water conditions to obtain an aqueous solution of a compound a, and directly entering the next reaction without post-treatment after the reaction is finished; adding a reducing agent alkaline water system into the aqueous solution of the compound a, controlling the temperature to react, controlling the temperature to adjust the pH value to 5-5.5 after the reaction is finished, extracting with n-butyl alcohol, and drying to obtain an n-butyl alcohol solution of a compound b, and directly entering the next reaction step; wherein the reducing agent is one of sodium borohydride and potassium borohydride; dropwise adding thionyl chloride into an n-butyl alcohol solution of the compound b, controlling the temperature to react after dropwise adding is ended, and concentrating to remove the solvent and unreacted thionyl chloride after the reaction is ended, so as to obtain a compound c; carrying out Dieckmann condensation reaction on the compound c at controlled temperature under the condition of organic alkali by using toluene as a solvent, carrying out hydrochloric acid quenching reaction after the reaction is finished, and directly carrying out next-step reaction after extracting and removing impurities from a water phase containing a hydrochloride solution of a compound d by using toluene; and carrying out a decarboxylation reaction on the compound d in a hydrochloric acid aqueous solution at controlled temperature, after the reaction is finished, adjusting the pH value to 10-13, extracting, and salifying to obtain a target compound TM, namely 3-quinuclidinone hydrochloride. The preparation method of 3-quinuclidinone hydrochloride provided by the invention has the advantages of economical and easily available raw materials, mild reaction conditions, efficient reaction, simple operation and low cost, and is suitable for industrial application.

The invention discloses application of bismuth vanadium tetraoxide as a photocatalyst in preparation of allantoin. According to the method, a decahedral single crystal micron material bismuth vanadium tetroxide is used as a photocatalyst, uric acid is used as a substrate, a photocatalytic reaction is performed under the irradiation of visible light, and uric acid is oxidized, hydrolyzed, decarboxylated and converted into allantoin; compared with a traditional chemical synthesis method, the method has the advantages that the bismuth vanadium tetraoxide serves as a photocatalyst, uric acid is converted into allantoin through photocatalytic reaction, selective activation of chemical bonds is achieved through directional regulation and control of photo-induced electron-hole pairs, and the method is mild in reaction condition, low in energy consumption and the like.

Improved conductive ink compositions are provided. The improved conductive ink compositions include a silver complex formed by mixing a silver carboxylate, specifically a silver decanoate, a cyclic azasilane adhesion promoter, and at least one dissolving agent. The silver carboxylate of the subject ink compositions is decarboxylated at a temperature of 250 °C or less, optionally in the presence of an acid stabilizer or non-acid stabilizer, to form a conductive structure. Methods of making the compositions and methods of forming conductive structures from the compositions, including methods where the disclosed compositions are applied to a substrate by various techniques, are also provided.

The application belongs to the technical field of preparation and application of spermidine, and particularly relates to application of fusarium NF01 in preparation of spermidine and catalysis of lignite liquefaction. The fusarium NF01 is fusarium strain Fusarium sp. NF01. The application finds that the fusarium strain Fusarium sp. NF01 can secrete spermidine synthetase, and then catalyze putrescine and decarboxylated S-adenosyl methionine to biosynthesize spermidine through the spermidine synthetase, so that the spermidine acts on lignite, and then the lignite is liquefied, which can promote the technical progress and application expansion in the field of coal development.

The application belongs to the technical field of compound synthesis, and particularly relates to an alpha-ketoamide derivative and a preparation method thereof, wherein the preparation method of the alpha-ketoamide derivative comprises the following steps: S1, first, a graphite carbon rod electrode and a platinum sheet electrode are respectively assembled on two sides of a 10mL three-port glass bottle; S2, then, a magnetic son is added into the three-port glass bottle, the bottle mouths on two sides are sealed, the three-port glass bottle is transferred to a glove box for feeding, and benzoylformic acid, morpholine and 10mol% of ferrocene in 4mL hexafluoroisopropanol are sequentially added; S3, after the feeding is completed, the last bottle mouth of the three-port glass bottle is sealed, and a constant current of 3mA is introduced for electrolysis. The application realizes the amination reaction of alpha-keto acid by using an electrocatalytic decarboxylation strategy, selectively synthesizes alpha-ketoamide derivatives, and the reaction is suitable for primary amine compounds, secondary amine compounds, is also suitable for aromatic and aliphatic alpha-keto acids, and excellent functional group tolerance is exhibited.

The invention discloses a synthesis method of an inner piroxostat key intermediate and a synthesis method of inner piroxostat. The invention provides a novel synthesis method of an inner piroxostat key intermediate 5, 7-difluoro-1, 2, 3, 4-tetrahydronaphthalene-2-amine, which comprises the following steps: taking 3, 5-difluorobenzyl bromide as a raw material, carrying out substitution reaction on the 3, 5-difluorobenzyl bromide and methane tricarboxylic acid triethyl ester, then carrying out hydrolysis decarboxylation, adding 1, 2, 3, 4-tetrahydronaphthalene-2-amine, and carrying out reaction to obtain the 5, 7-difluoro-1, 2, 3, 4-tetrahydronaphthalene-2-amine. The preparation method comprises the following steps: substituting 1, 2-diiodoethane, catalyzing carbon-hydrogen activation and ring closing by tetrakis (triphenylphosphine) palladium, hydrolyzing and decarboxylating, amidating, and carrying out Hofmann degradation reaction to obtain a target intermediate. The method has the advantages of cheap and easily available raw materials, simple synthesis and high yield, avoids the use of ethylene, sodium azide and other reagents, and is green and safe. The invention provides a method for further synthesizing the endopiroxostat based on the synthesis method, the method comprises a novel endopiroxostat hydrochloride chiral resolution method, the chiral pure endopiroxostat is conveniently prepared through a chiral preparative column, and the ee value is 100%.

The invention discloses a preparation method of a dapagliflozin intermediate 5-bromine-2-chlorine-4 '-ethyoxyl diphenylmethane, which comprises the following steps: carrying out nucleophilic substitution reaction on 4-bromine-1-chlorine-2-fluorobenzene and 4-ethyoxyl phenylacetate, and then hydrolyzing and decarboxylating to obtain the dapagliflozin intermediate 5-bromine-2-chlorine-4'-ethyoxyl diphenylmethane. By optimizing the preparation route, the reaction utilization rate, the product yield and the product purity of the raw materials are improved, high-risk and high-pollution chemicals are prevented from being used, and the method is convenient to operate, safe, environmentally friendly, efficient in reaction and beneficial to industrial implementation.