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Synthesis method of 3,5-dihalogenated-2-pentanone

A synthetic method, a dihalogenated technology, applied in the field of synthesis of 3,5-dihalogenated-2-pentanone, which can solve the problems of high production safety risks, achieve high atom utilization, less waste, and simple reaction conditions Effect

Active Publication Date: 2020-05-29
DALIAN JOIN KING FINE CHEM CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The raw material methyl vinyl ketone used in this route is highly toxic, and the production safety risk is relatively high (see: J.Chem.Soc., Chem.Commun., 1983, 1446)

Method used

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  • Synthesis method of 3,5-dihalogenated-2-pentanone
  • Synthesis method of 3,5-dihalogenated-2-pentanone
  • Synthesis method of 3,5-dihalogenated-2-pentanone

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0022] In the first step, add methyl acetoacetate 1a (116.1g, 1.0mol), dichloroethane (247.4g, 2.5eq) and β-cyclodextrin (22.7g, 0.02eq) into a 2L reaction flask, heat and stir To 40°C, slowly add 40% sodium hydroxide solution (400.0g, 4.0eq) from the dropping funnel, it takes 1.0h to finish dropping, control the temperature during the dropping process at 40-45°C, continue to keep stirring for 2.0 h.

[0023] Stop heating and drop to room temperature, separate the lye layer containing β-cyclodextrin for recycling, then separate the dichloroethane layer, add water to wash until neutral and directly use for ring-opening halogenation reaction, intermediate ( 2a) GC purity 97% (minus dichloroethane).

[0024] In the second step, chlorine gas (85.1 g, 1.2 mol) was introduced into the dichloroethane solution of the intermediate (2a) obtained above, and it took 2.0 hours to pass through. The temperature during the ventilation process was controlled at 0-5 ° C. After the ventilation ...

Embodiment 2

[0028] The first step is the same as in Example 1.

[0029] In the second step, bromine (175.8g, 1.1mol) was added dropwise to the dichloroethane solution of the intermediate (2a) obtained in the first step, and it took 2.0h to complete the dropwise addition, and the dropping process controlled the temperature at 0-5 ℃, after the drop is completed, continue to keep stirring for 1.0h. The dichloroethane solution of the obtained intermediate (3b) was directly used in the hydrolysis decarboxylation reaction, and the gas chromatography purity of the intermediate (3b) was 93% (deducting dichloroethane).

[0030] In the third step, the ethylene dichloride solution of the intermediate (3b) is transferred to the dropping funnel, and slowly added dropwise to a reaction flask preheated to 80° C. with 20% hydrochloric acid (182.5g, 1.0eq), which takes time After 1.0h of dripping, the mixture was kept stirring for 2.0h.

[0031] Stop heating and cool down to room temperature, separate d...

Embodiment 3

[0033] The first step is the same as in Example 1.

[0034] In the second step, a solution prepared from iodine (279.2 g, 1.1 mol) and 300 g of dichloroethane was added dropwise to the dichloroethane solution of the intermediate (2a) obtained in the first step, and it took about 2.0 hours to complete the dropwise addition. During the dropping process, the temperature was controlled at 0-5°C, and the stirring was continued for 1.0 h after the dropping was completed. The dichloroethane solution of the obtained intermediate (3c) was directly used in the hydrolysis decarboxylation reaction, and the gas chromatography purity of the intermediate (3c) was 81% (dichloroethane was deducted).

[0035] In the third step, the ethylene dichloride solution of the intermediate (3c) is transferred to the dropping funnel, and slowly added dropwise to a reaction flask preheated to 80° C. with 20% hydrochloric acid (182.5g, 1.0eq), which takes time After 1.0h of dripping, the mixture was kept s...

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Abstract

The invention discloses a synthetic method of 3,5-dihalogenated-2-pentanone, and belongs to the technical field of organic chemistry. According to the method, acetoacetate is taken as a raw material,and cyclopropanation, ring-opening halogenation and hydrolysis decarboxylation reactions are carried out successively so as to obtain 3,5-dihalogenated-2-pentanone. The method has the advantages of simple and accessible raw materials, high atom utilization ratio in the halogenation step and fewer wastes. The reaction conditions of all steps are simple, purification is not needed in the process, continuous feeding can be achieved, cyclic application of the cyclopropanation catalyst can be achieved, and potential industrial amplification prospects are achieved.

Description

Technical field: [0001] The invention belongs to the field of organic chemistry, and in particular relates to a synthesis method of 3,5-dihalo-2-pentanone. Background technique: [0002] 3,5-Dihalo-2-pentanone is widely used in the fields of medicine and pesticide. For example, further intramolecular cyclization of this compound can prepare 1-acetyl-1-chlorocyclopropane, which is an important intermediate for the synthesis of fungicide prothioconazole (see: CN106278850); further cyclization with potassium thiocyanate The sedative-hypnotic drug clomethiazole can be prepared (see: Chinese Journal of Pharmaceutical Industry, 2006, 37, 441). [0003] The synthetic method that has been reported in the existing literature: 1) using acetyl-γ-butyrolactone as raw material, after chlorination and esterification, and further decarboxylation reaction under the action of concentrated hydrochloric acid to obtain the target product 3,5-dihalogen On behalf of -2-pentanone. This route ha...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07C45/67C07C49/16C07C67/343C07C69/757C07C67/307C07C69/716
CPCC07C45/676C07C67/343C07C67/307C07C2601/02C07C69/757C07C69/716C07C49/16
Inventor 戴耀王旭艳梁全德刘玲玲王荣良王延波
Owner DALIAN JOIN KING FINE CHEM CO LTD
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