JPS55141424A - Production of reduction type coenzyme q - Google Patents
Production of reduction type coenzyme qInfo
- Publication number
- JPS55141424A JPS55141424A JP245080A JP245080A JPS55141424A JP S55141424 A JPS55141424 A JP S55141424A JP 245080 A JP245080 A JP 245080A JP 245080 A JP245080 A JP 245080A JP S55141424 A JPS55141424 A JP S55141424A
- Authority
- JP
- Japan
- Prior art keywords
- reaction
- dimethoxy
- isopropyl ether
- formula
- production
- 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)
Abstract
PURPOSE: The reaction between 2,3-dimethoxy-5-methylhydroquinone-(1,4) and prenyl alcohol is conducted in isopropyl ether in the presence of boron trifluorideetherate complex to produce title compound useful as an intermediate of coenzyme Q in high yield.
CONSTITUTION: The reaction of 2,3-dimethoxy-5-methylhydroquinone-(1,4) of formula I (R is H, acyl) or its acyl derivative with prenyl alcohol of formula II (n is 0 or positive integral number), its isomer or its reactive derivative is effected in isopropyl ether in the presence of boron trifluorideetherate complex to produce 2,3- dimethoxy-5-methyl-6-prenylhydroquinone of formula III and its acyl derivative. This reaction proceeds in homogenous system and the reaction temperature is preferably 30W60°C.
EFFECT: The control of the reaction temperature is simple. Isopropyl ether is excellent not only as the reaction solvent but also as the extraction solvent. The recovery also is simple.
COPYRIGHT: (C)1980,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP245080A JPS55141424A (en) | 1980-01-10 | 1980-01-10 | Production of reduction type coenzyme q |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP245080A JPS55141424A (en) | 1980-01-10 | 1980-01-10 | Production of reduction type coenzyme q |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP50148477A Division JPS5915894B2 (en) | 1975-12-15 | 1975-12-15 | Hokouso Q Noseizou Hohou |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS55141424A true JPS55141424A (en) | 1980-11-05 |
JPS5742613B2 JPS5742613B2 (en) | 1982-09-09 |
Family
ID=11529610
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP245080A Granted JPS55141424A (en) | 1980-01-10 | 1980-01-10 | Production of reduction type coenzyme q |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS55141424A (en) |
-
1980
- 1980-01-10 JP JP245080A patent/JPS55141424A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5742613B2 (en) | 1982-09-09 |
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