JPS557206A - Preparation of optically active ester - Google Patents
Preparation of optically active esterInfo
- Publication number
- JPS557206A JPS557206A JP7804878A JP7804878A JPS557206A JP S557206 A JPS557206 A JP S557206A JP 7804878 A JP7804878 A JP 7804878A JP 7804878 A JP7804878 A JP 7804878A JP S557206 A JPS557206 A JP S557206A
- Authority
- JP
- Japan
- Prior art keywords
- compound
- optically active
- formula
- prochiral
- alcohol
- 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.)
- Granted
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
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Abstract
PURPOSE: To obtain the title compound with high optical purity in high yield, by the hydroesterification of a prochiral ethylenic unsaturated compound with CO and an alcohol using an optically active complex catalyst comprising a Pd compound and an optically active diphosphine.
CONSTITUTION: A prochiral compound having a carbon double bond, e.g. α- methylstyrene, 1-butene, etc. is hydroesterified with CO and an alcohol, using a complex catalyst of optically active diphosphine of formula I (DBP is 5H-dibenzophosphoryl of formula II; vicinal asymmetric carbons with the mark × have the same configuration, and R and R' may together form a 4-5 membered carbon ring or heterocyclic ring) and a Pd compound, e.g. PdCl 2(PhCN)2, to give the objective compound, e.g. 3-phenylisopropyl butylate. As the compound of formula I, e.g. (-)-trans-1, 2-bis(5H-dibenzophosphorylmethyl)cyclobutane is used.
COPYRIGHT: (C)1980,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP53078048A JPS584705B2 (en) | 1978-06-29 | 1978-06-29 | Method for producing optically active 3-phenylbutyric acid ester |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP53078048A JPS584705B2 (en) | 1978-06-29 | 1978-06-29 | Method for producing optically active 3-phenylbutyric acid ester |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS557206A true JPS557206A (en) | 1980-01-19 |
JPS584705B2 JPS584705B2 (en) | 1983-01-27 |
Family
ID=13650956
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP53078048A Expired JPS584705B2 (en) | 1978-06-29 | 1978-06-29 | Method for producing optically active 3-phenylbutyric acid ester |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS584705B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5654250A (en) * | 1994-05-19 | 1997-08-05 | Shell Oil Company | Preparation of catalyst solution |
-
1978
- 1978-06-29 JP JP53078048A patent/JPS584705B2/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5654250A (en) * | 1994-05-19 | 1997-08-05 | Shell Oil Company | Preparation of catalyst solution |
Also Published As
Publication number | Publication date |
---|---|
JPS584705B2 (en) | 1983-01-27 |
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