Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Preparation method for (2Z,4E)11-methoxy-3,7,11-trimethyl-2,4-dodecadienoic acid isopropyl ester

A technology of isopropyl carbadienoate and dimethylformamide diisopropyl acetal, applied in (2Z,4E)11-methoxy-3,7,11-trimethyl-2,4 - The field of preparation of isopropyl dodecadienoate can solve the problems of reducing the effective active content of products, reducing the purity of active ingredients, shortening the shelf life of products, etc., and achieve the effects of enhanced operational feasibility, no transition metal residues, and extended shelf life

Active Publication Date: 2011-11-16
常州胜杰生命科技股份有限公司
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In the prior art, tetraalkyl titanate is often used as an esterification agent, and 11-methoxy-3,7,11-trimethyl-2,4-dodecadienoic acid is used as a reaction raw material, and the reaction temperature is Synthesize 11-methoxy-3,7,11-trimethyl-2,4-dodecadienoic acid isopropyl ester within the range of 110-200°C. In the prior art, the esterification agent is selected It is tetraalkyl titanate, and there are remaining organic titanium during the esterification reaction with the raw material 11-methoxy-3,7,11-trimethyl-2,4-dodecadienoic acid acid salt, need additional solvent to dilute, wash with sulfuric acid, then wash with glycolic acid and potassium carbonate solution, remove the titanate and then concentrate to remove the added solvent to obtain the final product, resulting in very cumbersome post-processing
The prior art obtains a product weight yield of 100%, but the cis-isomer content is as high as 2.5-4%.
At the same time, with tetraalkyl titanate as the esterification agent, although the transition metal titanium ions have a series of washing and removal operations in the post-treatment process, there will always be a small amount of residue in the product, which will cause the finished product to be formed during storage. Type conversion from trans to cis shortens the shelf life of the product
Since the cis product is an ineffective component as an insect inhibitor, the high-temperature reaction and the residual catalysis of trace transition metal ions cause the conversion of the trans to the cis configuration, reducing the purity of the active ingredients of the product, thereby reducing the product quality. The effective active content of

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0015] 3L four-necked flask, protected with dry nitrogen, put in (2Z, 4E)11-methoxy-3,7,11-trimethyl-2,4-dodecadienoic acid, and then put in Freshly distilled N,N-dimethylformamide diisopropyl acetal, heated to 80°C, reacted for 2h, liquid spectrum monitoring, reaction to acid <1%, vacuum distillation to remove unreacted acetal, The remaining product in the bottle (2Z, 4E) 11-methoxy-3,7,11-trimethyl-2,4-dodecadienoic acid isopropyl ester 882g, weight yield: 104%.

[0016] The content of the trans configuration ((2Z, 4E) configuration) of the product is 96.81%, and the content of the cis configuration ((2E, 4E) configuration) is 1.31%.

[0017] The amount of N,N-dimethylformamide diisopropyl acetal is 1106g, 6.32mol;

[0018] The amount of (2Z, 4E)11-methoxy-3,7,11-trimethyl-2,4-dodecadienoic acid is 847g, 3.16mol.

[0019] The above-mentioned N,N-dimethylformamide diisopropyl acetal and (2Z,4E)11-methoxy-3,7,11-trimethyl-2,4-dodecadienoic acid The molar ratio is 2:1.

Embodiment 2

[0021] 3L four-necked flask, protected with dry nitrogen, put in (2Z, 4E)11-methoxy-3,7,11-trimethyl-2,4-dodecadienoic acid, and then put in Freshly distilled N,N-dimethylformamide diisopropyl acetal, heated to 80°C, reacted for 2h, liquid spectrum monitoring, reaction to acid <1%, vacuum distillation to remove unreacted acetal, The remaining product in the bottle (2Z, 4E) 11-methoxy-3,7,11-trimethyl-2,4-dodecadienoic acid isopropyl ester 882g, weight yield: 104%.

[0022] The content of the trans configuration ((2Z, 4E) configuration) of the product is 96.90%, and the content of the cis configuration ((2E, 4E) configuration) is 1.29%.

[0023] The amount of N,N-dimethylformamide diisopropyl acetal is 1382g, 7.9mol;

[0024] The amount of (2Z, 4E)11-methoxy-3,7,11-trimethyl-2,4-dodecadienoic acid is 847g, 3.16mol.

[0025] The above-mentioned N,N-dimethylformamide diisopropyl acetal and (2Z,4E)11-methoxy-3,7,11-trimethyl-2,4-dodecadienoic acid The molar ratio is 2.5:1.

Embodiment 3

[0027] 3L four-necked flask, protected with dry nitrogen, put in (2Z, 4E)11-methoxy-3,7,11-trimethyl-2,4-dodecadienoic acid, and then put in The freshly distilled N,N-dimethylformamide diisopropyl acetal was heated to 80° C., reacted for 5 hours, and the liquid spectrum monitored the reaction until the acid was less than 1%. Vacuum distillation to remove unreacted acetal, the remaining product in the bottle (2Z, 4E) 11-methoxy-3,7,11-trimethyl-2,4-dodecadienoic acid isopropyl ester 882g , Weight yield: 104%.

[0028] The content of the trans configuration ((2Z, 4E) configuration) of the product is 96.62%, and the content of the cis configuration ((2E, 4E) configuration) is 1.34%.

[0029] The amount of N,N-dimethylformamide diisopropyl acetal is 830g, 4.74mol;

[0030] The amount of (2Z, 4E)11-methoxy-3,7,11-trimethyl-2,4-dodecadienoic acid is 847g, 3.16mol.

[0031] The above-mentioned N,N-dimethylformamide diisopropyl acetal and (2Z,4E)11-methoxy-3,7,11-trimethyl-2,4-dodecadienoic...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention discloses a preparation method for (2Z,4E)11-methoxy-3,7,11-trimethyl-2,4-dodecadienoic acid isopropyl ester. The method is characterized in that: (2Z,4E)11-methoxy-3,7,11-trimethyl-2,4-dodecadienoic acid is used as a raw material; N, N-dimethylformamide diisopropyl acetal is used as an esterification reagent which reacts with (2Z,4E)11-methoxy-3,7,11-trimethyl-2,4-dodecadienoic acid at a temperature in a range of 80 to 100 DEG C for 2 to 5 hours; the reaction is stopped when the content of acid in the raw material is less than 1%; the product of the reaction is subjected to aftertreatment so as to obtain the desired target product. The beneficial effects of the invention are as follows: compared to the prior art, yield of the target product is substantially enhanced; energyconservation in the whole process of preparation is realized; the aftertreatment is easy and operable.

Description

Technical field [0001] The invention relates to a preparation method of (2Z, 4E)11-methoxy-3,7,11-trimethyl-2,4-dodecadienoic acid isopropyl. Background technique [0002] (2Z,4E)11-Methoxy-3,7,11-trimethyl-2,4-dodecadienoic acid isopropyl ester, commonly known as (S)-Methoprin, is an effective Insect growth inhibitor. It is a new type of specific insecticide that targets the insect's unique growth and development system. After the hormone enters the mosquito's body, it causes the mosquito's underdevelopment, loss of attack and reproduction ability, and achieves the purpose of reducing mosquitoes from the source. In the prior art, tetraalkyl titanate is often used as the esterification agent, and 11-methoxy-3,7,11-trimethyl-2,4-dodecadienoic acid is used as the reaction material. The reaction temperature It is controlled within the range of 110~200℃ to synthesize 11-methoxy-3,7,11-trimethyl-2,4-dodecadienoic acid isopropyl ester. In the prior art, the esterification agent is se...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): C07C69/734C07C67/24
Inventor 苏衡李海燕韩永青王加高
Owner 常州胜杰生命科技股份有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products