GB842725A - Methods of preparing diketodicarboxylic acid esters, and diketodicarboxylic acid esters when prepared by said methods - Google Patents
Methods of preparing diketodicarboxylic acid esters, and diketodicarboxylic acid esters when prepared by said methodsInfo
- Publication number
- GB842725A GB842725A GB32499/56A GB3249956A GB842725A GB 842725 A GB842725 A GB 842725A GB 32499/56 A GB32499/56 A GB 32499/56A GB 3249956 A GB3249956 A GB 3249956A GB 842725 A GB842725 A GB 842725A
- Authority
- GB
- United Kingdom
- Prior art keywords
- diketodicarboxylic
- acid esters
- methods
- prepared
- formula
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/67—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids
- C07C69/716—Esters of keto-carboxylic acids or aldehydo-carboxylic acids
Abstract
Diketodicarboxylic acid esters of the general formula p YOOC.C.(X)(X1).CO.CH2.CO.COOZ are prepared by condensing the methyl or ethyl ester of a disubstituted acetoacetic acid of the formula YOOC.C(X)(X1).CO.CH3 with a dialkyl oxalate of the formula ZOOC-COOZ in the presence of sodium or potassium alcoholate, where X,X1 and Z are identical or different organic hydrocarbon radicals with 1-5 carbon atoms with straight or branched chains, saturated or unsaturated and Y is a methyl or ethyl group. The condensation may be effected at room temperature or preferably at 30 to 40 DEG C. The alcoholate used is preferably derived from the same alcohol as the oxalate. The products are useful as insecticides and repellents.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CS842725X | 1955-10-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB842725A true GB842725A (en) | 1960-07-27 |
Family
ID=5456030
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB32499/56A Expired GB842725A (en) | 1955-10-27 | 1956-10-25 | Methods of preparing diketodicarboxylic acid esters, and diketodicarboxylic acid esters when prepared by said methods |
Country Status (2)
Country | Link |
---|---|
FR (1) | FR1161259A (en) |
GB (1) | GB842725A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1987007265A1 (en) * | 1986-05-29 | 1987-12-03 | E.I. Du Pont De Nemours And Company | Acylation and sulfonation of silylketene acetals |
US4983679A (en) * | 1986-05-29 | 1991-01-08 | E. I. Dupont De Nemours And Company | β-(keto or sulfonyl)esters from reaction of silylketene acetal and acyl or sulfonyl compound |
US5110869A (en) * | 1986-05-29 | 1992-05-05 | E. I. Du Pont De Nemours And Company | β-(keto or sulfonyl)esters from reaction of silyketene acetal and acyl or sulfonyl compound |
US5260424A (en) * | 1986-05-29 | 1993-11-09 | E. I. Du Pont De Nemours And Company | B-(keto or sulfonyl) esters from reaction of silylketene acetal and acyl or sulfonyl compound |
CN111533655A (en) * | 2020-05-31 | 2020-08-14 | 广东工业大学 | Preparation method of long-carbon-chain keto dicarboxylic ester |
-
1956
- 1956-10-25 FR FR1161259D patent/FR1161259A/en not_active Expired
- 1956-10-25 GB GB32499/56A patent/GB842725A/en not_active Expired
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1987007265A1 (en) * | 1986-05-29 | 1987-12-03 | E.I. Du Pont De Nemours And Company | Acylation and sulfonation of silylketene acetals |
US4983679A (en) * | 1986-05-29 | 1991-01-08 | E. I. Dupont De Nemours And Company | β-(keto or sulfonyl)esters from reaction of silylketene acetal and acyl or sulfonyl compound |
US5110869A (en) * | 1986-05-29 | 1992-05-05 | E. I. Du Pont De Nemours And Company | β-(keto or sulfonyl)esters from reaction of silyketene acetal and acyl or sulfonyl compound |
US5260424A (en) * | 1986-05-29 | 1993-11-09 | E. I. Du Pont De Nemours And Company | B-(keto or sulfonyl) esters from reaction of silylketene acetal and acyl or sulfonyl compound |
CN111533655A (en) * | 2020-05-31 | 2020-08-14 | 广东工业大学 | Preparation method of long-carbon-chain keto dicarboxylic ester |
CN111533655B (en) * | 2020-05-31 | 2022-09-02 | 广东工业大学 | Preparation method of long-carbon-chain keto dicarboxylic ester |
Also Published As
Publication number | Publication date |
---|---|
FR1161259A (en) | 1958-08-25 |
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