JPS5738733A - Preparation of novel compound - Google Patents
Preparation of novel compoundInfo
- Publication number
- JPS5738733A JPS5738733A JP9698881A JP9698881A JPS5738733A JP S5738733 A JPS5738733 A JP S5738733A JP 9698881 A JP9698881 A JP 9698881A JP 9698881 A JP9698881 A JP 9698881A JP S5738733 A JPS5738733 A JP S5738733A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- compound
- copper
- amine
- pref
- 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
NEW MATERIAL:The compound of formula I (R is group of formula II, formula III, or formula IV).
EXAMPLE: 2,6,10,15,19,23-Hexamethyltetracosa-11,13-diyne-6,18-diene-10,15-diol.
USE: An intermediate for the synthesis of squalane which is useful as a component of cosmetics, lubricant, etc.
PROCESS: The compound of formula I can be prepared by the oxidative coupling of the compound of formula V with molecular oxygen in the presence of an amine and 0.1W20mol%, based on the compound of formula V, of a copper compound. The amine is pref. a hetero-cyclic aromatic amine such as pyridine, picoline, etc. and its amount is pref. 5W50wt% based on the compound of formula V. The copper compound is an univalent copper salt (e.g. cuprous chloride) or a bivalent copper carboxylate (e.g. cupric acetate), and its amount is 0.5W10mol% based on the compound of formula V.
COPYRIGHT: (C)1982,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56096988A JPS5935904B2 (en) | 1981-06-22 | 1981-06-22 | Method for producing new compounds |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56096988A JPS5935904B2 (en) | 1981-06-22 | 1981-06-22 | Method for producing new compounds |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5738733A true JPS5738733A (en) | 1982-03-03 |
JPS5935904B2 JPS5935904B2 (en) | 1984-08-31 |
Family
ID=14179582
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56096988A Expired JPS5935904B2 (en) | 1981-06-22 | 1981-06-22 | Method for producing new compounds |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5935904B2 (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6289354U (en) * | 1985-11-25 | 1987-06-08 | ||
WO1999030822A1 (en) * | 1997-12-16 | 1999-06-24 | Exxon Research And Engineering Company | Group 11 transition metal amine catalysts for olefin polymerization |
US6037297A (en) * | 1997-12-16 | 2000-03-14 | Exxon Research And Engineering Co. | Catalyst complexes and polymers therefrom |
US6180788B1 (en) | 1997-12-16 | 2001-01-30 | Exxon Research And Engineering Company | Catalyst compositions |
US6417303B1 (en) | 1997-12-16 | 2002-07-09 | Exxonmobil Research And Engineering Company | Substantially linear copolymers |
US6501000B1 (en) | 2000-04-04 | 2002-12-31 | Exxonmobil Research And Engineering Company | Late transition metal catalyst complexes and oligomers therefrom |
US6689928B2 (en) | 2000-04-04 | 2004-02-10 | Exxonmobil Research And Engineering Company | Transition metal complexes and oligomers therefrom |
JP2007230931A (en) * | 2006-03-02 | 2007-09-13 | Nagoya Industrial Science Research Inst | Method for producing 1,3-diyne compound |
JP2015536304A (en) * | 2012-10-11 | 2015-12-21 | ディーエスエム アイピー アセッツ ビー.ブイ. | Stepwise hydrogenation of specific isoprenoids |
-
1981
- 1981-06-22 JP JP56096988A patent/JPS5935904B2/en not_active Expired
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6289354U (en) * | 1985-11-25 | 1987-06-08 | ||
WO1999030822A1 (en) * | 1997-12-16 | 1999-06-24 | Exxon Research And Engineering Company | Group 11 transition metal amine catalysts for olefin polymerization |
US6037297A (en) * | 1997-12-16 | 2000-03-14 | Exxon Research And Engineering Co. | Catalyst complexes and polymers therefrom |
US6180788B1 (en) | 1997-12-16 | 2001-01-30 | Exxon Research And Engineering Company | Catalyst compositions |
US6417303B1 (en) | 1997-12-16 | 2002-07-09 | Exxonmobil Research And Engineering Company | Substantially linear copolymers |
US6501000B1 (en) | 2000-04-04 | 2002-12-31 | Exxonmobil Research And Engineering Company | Late transition metal catalyst complexes and oligomers therefrom |
US6689928B2 (en) | 2000-04-04 | 2004-02-10 | Exxonmobil Research And Engineering Company | Transition metal complexes and oligomers therefrom |
JP2007230931A (en) * | 2006-03-02 | 2007-09-13 | Nagoya Industrial Science Research Inst | Method for producing 1,3-diyne compound |
JP2015536304A (en) * | 2012-10-11 | 2015-12-21 | ディーエスエム アイピー アセッツ ビー.ブイ. | Stepwise hydrogenation of specific isoprenoids |
Also Published As
Publication number | Publication date |
---|---|
JPS5935904B2 (en) | 1984-08-31 |
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