JPS5495502A - Preparation of 3-methyl-2-buten-1-ol - Google Patents
Preparation of 3-methyl-2-buten-1-olInfo
- Publication number
- JPS5495502A JPS5495502A JP88078A JP88078A JPS5495502A JP S5495502 A JPS5495502 A JP S5495502A JP 88078 A JP88078 A JP 88078A JP 88078 A JP88078 A JP 88078A JP S5495502 A JPS5495502 A JP S5495502A
- Authority
- JP
- Japan
- Prior art keywords
- buten
- methyl
- preparation
- prenol
- isomerizing
- 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: To obtain the title compound (prenol) useful as a raw material of terpene derivatives, etc., economically, by isomerizing 3-methyl-3-buten-1-ol in the presence of a specific low-cost catalyst.
CONSTITUTION: 3-methyl-2-buten-1-ol (prenol) is obtained by isomerizing 3-methyl- 3-buten-1-ol using an alkali metal hydroxide or an alkali metal alcoholate, e.g. pottasium hydroxide, as a catalyst. Only isoprene which is easily separable, is obtained as a by-product.
COPYRIGHT: (C)1979,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP88078A JPS5495502A (en) | 1978-01-10 | 1978-01-10 | Preparation of 3-methyl-2-buten-1-ol |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP88078A JPS5495502A (en) | 1978-01-10 | 1978-01-10 | Preparation of 3-methyl-2-buten-1-ol |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5495502A true JPS5495502A (en) | 1979-07-28 |
Family
ID=11485977
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP88078A Pending JPS5495502A (en) | 1978-01-10 | 1978-01-10 | Preparation of 3-methyl-2-buten-1-ol |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5495502A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0839897A1 (en) * | 1996-10-30 | 1998-05-06 | Rinoru Oil Mills Co., Ltd. | Method for producing conjugated linoleic acid |
CN109721470A (en) * | 2018-12-29 | 2019-05-07 | 中触媒新材料股份有限公司 | A kind of method that serialization prepares prenol |
WO2021142938A1 (en) * | 2020-01-17 | 2021-07-22 | 浙江新和成股份有限公司 | Ceramic corrugated plate catalyst coated with metal oxide, preparation therefor, and use thereof in preparing key intermediate of citral |
-
1978
- 1978-01-10 JP JP88078A patent/JPS5495502A/en active Pending
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0839897A1 (en) * | 1996-10-30 | 1998-05-06 | Rinoru Oil Mills Co., Ltd. | Method for producing conjugated linoleic acid |
US5986116A (en) * | 1996-10-30 | 1999-11-16 | Rinoru Oil Mills Co., Ltd. | Method for producing conjugated linoleic acid |
CN109721470A (en) * | 2018-12-29 | 2019-05-07 | 中触媒新材料股份有限公司 | A kind of method that serialization prepares prenol |
CN109721470B (en) * | 2018-12-29 | 2022-03-25 | 中触媒新材料股份有限公司 | Method for continuously preparing isopentenol |
WO2021142938A1 (en) * | 2020-01-17 | 2021-07-22 | 浙江新和成股份有限公司 | Ceramic corrugated plate catalyst coated with metal oxide, preparation therefor, and use thereof in preparing key intermediate of citral |
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