JPS5470257A - Preparation of optically active pantolactone - Google Patents
Preparation of optically active pantolactoneInfo
- Publication number
- JPS5470257A JPS5470257A JP13353677A JP13353677A JPS5470257A JP S5470257 A JPS5470257 A JP S5470257A JP 13353677 A JP13353677 A JP 13353677A JP 13353677 A JP13353677 A JP 13353677A JP S5470257 A JPS5470257 A JP S5470257A
- Authority
- JP
- Japan
- Prior art keywords
- pantolactone
- rhodium complex
- optically active
- butyrolactone
- oxo
- 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 obtain the title substance which is a raw material for calcium pantothenate, by catalytic asymmetric hydrogenation of 4,4-dimethyl-3-oxo-γ-butyrolactone, using a rhodium complex having an N-acylpyrrolidinophosphine as a ligand, as a catalyst.
CONSTITUTION: 4,4-Dimethyl-3-oxo-γ-butyrolactone is dissolved in a solvent, e.g. benzene, ether, etc. and hydrogenated in the presence of 0.01W0.5mol% of a rhodium complex at room temperature or at high temperature and pressure of 20W 60°C and several to scores of atmospheres to shorten the reaction time, thus forming the desired compound. The rhodium complex has an N-acylpyrrolidino phosphine of formula (the star is optically active site; R1, R2, R3, and R4 are alkyl or aromatic groups; R5, R6, and R7 are H, alkyl, or aromatic groups) as a ligand. The resulting pantolactone is recrystallized simply to form D-(-)-pantolactone of optical purity 100%.
COPYRIGHT: (C)1979,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13353677A JPS5470257A (en) | 1977-11-09 | 1977-11-09 | Preparation of optically active pantolactone |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13353677A JPS5470257A (en) | 1977-11-09 | 1977-11-09 | Preparation of optically active pantolactone |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5470257A true JPS5470257A (en) | 1979-06-05 |
Family
ID=15107094
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13353677A Pending JPS5470257A (en) | 1977-11-09 | 1977-11-09 | Preparation of optically active pantolactone |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5470257A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR19980059286A (en) * | 1996-12-31 | 1998-10-07 | 박영구 | Method for preparing D-(-)-pantolactone |
-
1977
- 1977-11-09 JP JP13353677A patent/JPS5470257A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR19980059286A (en) * | 1996-12-31 | 1998-10-07 | 박영구 | Method for preparing D-(-)-pantolactone |
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