JPS552628A - Isomerization of piperitol - Google Patents
Isomerization of piperitolInfo
- Publication number
- JPS552628A JPS552628A JP7476678A JP7476678A JPS552628A JP S552628 A JPS552628 A JP S552628A JP 7476678 A JP7476678 A JP 7476678A JP 7476678 A JP7476678 A JP 7476678A JP S552628 A JPS552628 A JP S552628A
- Authority
- JP
- Japan
- Prior art keywords
- trans
- piperitol
- cis
- catalyst
- complex
- 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
Abstract
PURPOSE: To prepare a mixture of cis- and trans-piperitols, in a short time, by the catalystic isomerization of cis- or trans-piperitol using a specific Co-phosphine complex as an isomerication catalyst.
CONSTITUTION: Cis or trans-piperitol is treated for a short time, with a catalyst comprising a low-valency Co-complex coordinated with a phosphine ligand having a coordination number of 2, to afford a mixture of cis-and trans-piperitols. The catalyst can be prepared by reacting a low-valency Co-olefin complex [pref. bivalent Co salt or a bivalent Co chelate compound (e.g. Co-acetylacetonate, etc.)] with a phosphine ligand having a coordination number of 2, e.g. 1,1'-bis-(diphenylphosphino)ferrocene, etc., in an organic solvent.
USE: Trans-piperitol is a raw material of menthol.
COPYRIGHT: (C)1980,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7476678A JPS552628A (en) | 1978-06-20 | 1978-06-20 | Isomerization of piperitol |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7476678A JPS552628A (en) | 1978-06-20 | 1978-06-20 | Isomerization of piperitol |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS552628A true JPS552628A (en) | 1980-01-10 |
JPS5735885B2 JPS5735885B2 (en) | 1982-07-31 |
Family
ID=13556722
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7476678A Granted JPS552628A (en) | 1978-06-20 | 1978-06-20 | Isomerization of piperitol |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS552628A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2368896B1 (en) * | 2010-03-01 | 2016-08-24 | ExxonMobil Chemical Patents Inc. | Mono-indenyl transition metal compounds and polymerization therewith |
-
1978
- 1978-06-20 JP JP7476678A patent/JPS552628A/en active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2368896B1 (en) * | 2010-03-01 | 2016-08-24 | ExxonMobil Chemical Patents Inc. | Mono-indenyl transition metal compounds and polymerization therewith |
Also Published As
Publication number | Publication date |
---|---|
JPS5735885B2 (en) | 1982-07-31 |
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