JPS5473710A - Production of 2-butene-1,4-diol derivative - Google Patents
Production of 2-butene-1,4-diol derivativeInfo
- Publication number
- JPS5473710A JPS5473710A JP13725577A JP13725577A JPS5473710A JP S5473710 A JPS5473710 A JP S5473710A JP 13725577 A JP13725577 A JP 13725577A JP 13725577 A JP13725577 A JP 13725577A JP S5473710 A JPS5473710 A JP S5473710A
- Authority
- JP
- Japan
- Prior art keywords
- butene
- catalyst
- copper compound
- production
- diol derivative
- 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.)
- Pending
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 hydration of a monoepoxide of 1,3-conjugated diene is conducted in the presence of water using a copper compound as a catalyst to form 2-butene-1,4- diol useful as an intermediate for chemicals in high selectivity.
CONSTITUTION: The hydration of a monoepoxide of 1,3-conjugated diene of formula I (R1-4 is H, hydrocarbyl wherein R1 and R4 may incorporate to form ring) is conducted in the presence of water a copper compound as a catalyst to produce 2-butene-1,4-diol derivative of formula II. As the copper compound, the bromide is suitable, especially cuprous bromide is preferred. The amount of the catalyst is 0.1W100wt% on the epoxide basis. The epoxide is, e.g., 3,4-epoxybutene-1. The reaction may be effected in an aqueous medium; however, the use of organic solvents is preferred. The reaction temperature is -10 -200°C.
COPYRIGHT: (C)1979,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13725577A JPS5473710A (en) | 1977-11-17 | 1977-11-17 | Production of 2-butene-1,4-diol derivative |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13725577A JPS5473710A (en) | 1977-11-17 | 1977-11-17 | Production of 2-butene-1,4-diol derivative |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5473710A true JPS5473710A (en) | 1979-06-13 |
Family
ID=15194377
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13725577A Pending JPS5473710A (en) | 1977-11-17 | 1977-11-17 | Production of 2-butene-1,4-diol derivative |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5473710A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01149741A (en) * | 1987-12-07 | 1989-06-12 | Nippon Mining Co Ltd | Production of 3-alkanols |
US5530167A (en) * | 1995-08-21 | 1996-06-25 | Eastman Chemical Company | Process for the preparation of 1,4-butenediol |
WO1998002404A1 (en) * | 1996-07-17 | 1998-01-22 | Eastman Chemical Company | PROCESS FOR THE PREPARATION OF 2-ALKENE-1,4-DIOLS AND 3-ALKENE-1,2-DIOLS FROM η,δ-EPOXYALKENES |
US5856591A (en) * | 1996-07-17 | 1999-01-05 | Eastman Chem Co | Process for the separation of 2-alkene-1,4-diols and 3-alkene-1,2-diols from catalysts |
WO1999011592A1 (en) * | 1997-09-04 | 1999-03-11 | The Dow Chemical Company | Process for the preparation of 1,4-butenediol from epoxybutene |
-
1977
- 1977-11-17 JP JP13725577A patent/JPS5473710A/en active Pending
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01149741A (en) * | 1987-12-07 | 1989-06-12 | Nippon Mining Co Ltd | Production of 3-alkanols |
JPH0446935B2 (en) * | 1987-12-07 | 1992-07-31 | Nippon Mining Co | |
US5530167A (en) * | 1995-08-21 | 1996-06-25 | Eastman Chemical Company | Process for the preparation of 1,4-butenediol |
WO1997007085A1 (en) * | 1995-08-21 | 1997-02-27 | Eastman Chemical Company | Process for the preparation of 1,4-butenediol |
WO1998002404A1 (en) * | 1996-07-17 | 1998-01-22 | Eastman Chemical Company | PROCESS FOR THE PREPARATION OF 2-ALKENE-1,4-DIOLS AND 3-ALKENE-1,2-DIOLS FROM η,δ-EPOXYALKENES |
US5856591A (en) * | 1996-07-17 | 1999-01-05 | Eastman Chem Co | Process for the separation of 2-alkene-1,4-diols and 3-alkene-1,2-diols from catalysts |
US5959162A (en) * | 1996-07-17 | 1999-09-28 | Eastman Chemical Company | Process for the preparation of 2-alkene-1,4-diols and 3-alkene-1,2-diols from γ,δ-epoxyalkenes |
WO1999011592A1 (en) * | 1997-09-04 | 1999-03-11 | The Dow Chemical Company | Process for the preparation of 1,4-butenediol from epoxybutene |
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