JPS57179133A - Synthesis of gamma-ketocarboxylic acid and its ester - Google Patents
Synthesis of gamma-ketocarboxylic acid and its esterInfo
- Publication number
- JPS57179133A JPS57179133A JP56062342A JP6234281A JPS57179133A JP S57179133 A JPS57179133 A JP S57179133A JP 56062342 A JP56062342 A JP 56062342A JP 6234281 A JP6234281 A JP 6234281A JP S57179133 A JPS57179133 A JP S57179133A
- Authority
- JP
- Japan
- Prior art keywords
- compound
- dihydrofuran
- ester
- formula
- ketocarboxylic acid
- 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.)
- Pending
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Abstract
PURPOSE: To prepare the titled compound useful as a precursor of cis-jasmine, etc., in high yield, by isomerizing dihydrofuran with a VIII-group transition metal hydride complex, reacting the product with an alcohol, and hydrolyzing the resultant tetrahydrofuran compound.
CONSTITUTION: A dihydrofuran compound of formulaI(R is alkyl or aryl; X is H, alkoxycarbonyl, alkyl or aryl) is used as the starting material, and is isomerized with a VIII-group transition metal hydride complex[e.g. dihydrido(carbonyl)tris(triphenylphosphine)-ruthenium]to obtain the dihydrofuran compound of formula II, which is converted to the tetrahydrofuran compound of formula III with an alcohol (e.g. methanol, ethanol, etc.) and then hydrolyzed to obtain the γ-ketocarboxylic acid of formula IV and its ester.
COPYRIGHT: (C)1982,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56062342A JPS57179133A (en) | 1981-04-27 | 1981-04-27 | Synthesis of gamma-ketocarboxylic acid and its ester |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56062342A JPS57179133A (en) | 1981-04-27 | 1981-04-27 | Synthesis of gamma-ketocarboxylic acid and its ester |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS57179133A true JPS57179133A (en) | 1982-11-04 |
Family
ID=13197346
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56062342A Pending JPS57179133A (en) | 1981-04-27 | 1981-04-27 | Synthesis of gamma-ketocarboxylic acid and its ester |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS57179133A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4851422A (en) * | 1985-04-30 | 1989-07-25 | Takeda Chemical Industries, Ltd. | Antibiotic 2-(3-oxo-2-isoxazolidinyl)-5-oxo-2-tetrahydrofuran-carboxylates |
-
1981
- 1981-04-27 JP JP56062342A patent/JPS57179133A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4851422A (en) * | 1985-04-30 | 1989-07-25 | Takeda Chemical Industries, Ltd. | Antibiotic 2-(3-oxo-2-isoxazolidinyl)-5-oxo-2-tetrahydrofuran-carboxylates |
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