JPS5686133A - Production of 3-pentenoic ester - Google Patents
Production of 3-pentenoic esterInfo
- Publication number
- JPS5686133A JPS5686133A JP16384079A JP16384079A JPS5686133A JP S5686133 A JPS5686133 A JP S5686133A JP 16384079 A JP16384079 A JP 16384079A JP 16384079 A JP16384079 A JP 16384079A JP S5686133 A JPS5686133 A JP S5686133A
- Authority
- JP
- Japan
- Prior art keywords
- butadiene
- isoquinoline
- pyridine
- catalyst
- hydroesterification
- 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: The hydroesterification of butadiene is effected in the presence of a small amount of cobalt carbonyl catalyst using a solvent mixture composed of pyridine and isoquinoline to produce the titled compound in high selectivity and yield with high industrial efficiency.
CONSTITUTION: The reaction between butadiene, carbon monoxide and a lower alcohol such as methanol is conducted in a solvent mixture composed of pyridine and isoquinoline in the presence of a cobalt carbonyl catalyst such as dicobalt octacarbonyl at 100W140°C under 100W300kg/cm2 carbon monoxide partial pressure to produce 3-pentenoic ester. The molar ratio of pyridine to isoquinoline is 1/(0.05W 10), preferably (0.1W5). The amount of the catalyst is 0.05W0.02mol/mol of butadiene.
EFFECT: A raw material, butadiene, is effectively utilized in low catalyst costs and the process is greatly significant as an industrial hydroesterification one.
COPYRIGHT: (C)1981,JPO&Japio
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP54163840A JPS5826901B2 (en) | 1979-12-17 | 1979-12-17 | Method for producing 3-pentenoic acid ester |
US06/199,332 US4332966A (en) | 1979-12-17 | 1980-10-21 | Process for producing 3-pentenoic esters |
DE19803040432 DE3040432C2 (en) | 1979-10-27 | 1980-10-27 | Process for the preparation of 3-pentenoic acid esters |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP54163840A JPS5826901B2 (en) | 1979-12-17 | 1979-12-17 | Method for producing 3-pentenoic acid ester |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5686133A true JPS5686133A (en) | 1981-07-13 |
JPS5826901B2 JPS5826901B2 (en) | 1983-06-06 |
Family
ID=15781742
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP54163840A Expired JPS5826901B2 (en) | 1979-10-27 | 1979-12-17 | Method for producing 3-pentenoic acid ester |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5826901B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS615051A (en) * | 1984-04-10 | 1986-01-10 | バスフ アクチエン ゲゼルシヤフト | Method of obtaining pentenoic acid c1-c4-alkyl ester |
-
1979
- 1979-12-17 JP JP54163840A patent/JPS5826901B2/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS615051A (en) * | 1984-04-10 | 1986-01-10 | バスフ アクチエン ゲゼルシヤフト | Method of obtaining pentenoic acid c1-c4-alkyl ester |
JPH0579658B2 (en) * | 1984-04-10 | 1993-11-04 | Basf Ag |
Also Published As
Publication number | Publication date |
---|---|
JPS5826901B2 (en) | 1983-06-06 |
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