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
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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...
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