JPS5671040A - Preparation of diacetoxybutene - Google Patents
Preparation of diacetoxybuteneInfo
- Publication number
- JPS5671040A JPS5671040A JP14691179A JP14691179A JPS5671040A JP S5671040 A JPS5671040 A JP S5671040A JP 14691179 A JP14691179 A JP 14691179A JP 14691179 A JP14691179 A JP 14691179A JP S5671040 A JPS5671040 A JP S5671040A
- Authority
- JP
- Japan
- Prior art keywords
- furan
- liquid
- butadiene
- catalyst layer
- acrolein
- 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
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
PURPOSE: To prepare the titled compound, by the continuous acetoxylation of butadiene in the presence of Pd and Te as catalysts under specific conditions while controlling the concentration of the by-produced furan, etc. in the reaction liquid, and discharging the furan from the system in one pass.
CONSTITUTION: The continuous acetoxylation of butadiene is carried out by passing butadiene, acetic acid and molecular oxygen through a catalyst layer comprising Pd and Te supported on activated charcoal, at 40W120°C and pressure of 30W 100kg/cm2, to obtain diacetoxybutene. The space velocity of the liquid and the O2- containing gas are 0.5W20hr-1 and 5W500hr-1, respectively. The concentrations (ppm) of furan and acrolein, which are by-products of the reaction produced as a result of oxidation of butadiene, in the liquid phase in the catalyst layer, are maintained to satisfy the formula wherein Fi and Ai are concentrations (ppm) of furan and acrolein in the liquid at the inlet of the catalyst layer and fO and AO are concentrations (ppm) of furan and acrolein in the liquid at the outlet of the catalyst layer.
COPYRIGHT: (C)1981,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14691179A JPS5671040A (en) | 1979-11-13 | 1979-11-13 | Preparation of diacetoxybutene |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14691179A JPS5671040A (en) | 1979-11-13 | 1979-11-13 | Preparation of diacetoxybutene |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5671040A true JPS5671040A (en) | 1981-06-13 |
JPS638930B2 JPS638930B2 (en) | 1988-02-25 |
Family
ID=15418347
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14691179A Granted JPS5671040A (en) | 1979-11-13 | 1979-11-13 | Preparation of diacetoxybutene |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5671040A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4714695A (en) * | 1985-04-18 | 1987-12-22 | The Standard Oil Company | Method for the preparation of high activity palladium based catalysts |
JPH01197457A (en) * | 1988-02-03 | 1989-08-09 | Daicel Chem Ind Ltd | Production of allyl acetate |
JP2008056951A (en) * | 2006-08-29 | 2008-03-13 | Mitsubishi Chemicals Corp | Nanocolloidal particle, method for producing the same, catalyst for diacetoxylation reaction of conjugated diene, and method for producing dicarboxylic acid diester |
WO2009142245A1 (en) * | 2008-05-21 | 2009-11-26 | 昭和電工株式会社 | METHOD FOR PRODUCING n-PROPYL ACETATE |
-
1979
- 1979-11-13 JP JP14691179A patent/JPS5671040A/en active Granted
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4714695A (en) * | 1985-04-18 | 1987-12-22 | The Standard Oil Company | Method for the preparation of high activity palladium based catalysts |
JPH01197457A (en) * | 1988-02-03 | 1989-08-09 | Daicel Chem Ind Ltd | Production of allyl acetate |
JP2008056951A (en) * | 2006-08-29 | 2008-03-13 | Mitsubishi Chemicals Corp | Nanocolloidal particle, method for producing the same, catalyst for diacetoxylation reaction of conjugated diene, and method for producing dicarboxylic acid diester |
WO2009142245A1 (en) * | 2008-05-21 | 2009-11-26 | 昭和電工株式会社 | METHOD FOR PRODUCING n-PROPYL ACETATE |
US8293936B2 (en) | 2008-05-21 | 2012-10-23 | Showa Denko Kabushiki Kaisha | Method for producing n-propyl acetate |
Also Published As
Publication number | Publication date |
---|---|
JPS638930B2 (en) | 1988-02-25 |
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