JPS5731660A - Beckmann rearrangement of cycloalkanone oxime - Google Patents
Beckmann rearrangement of cycloalkanone oximeInfo
- Publication number
- JPS5731660A JPS5731660A JP10513780A JP10513780A JPS5731660A JP S5731660 A JPS5731660 A JP S5731660A JP 10513780 A JP10513780 A JP 10513780A JP 10513780 A JP10513780 A JP 10513780A JP S5731660 A JPS5731660 A JP S5731660A
- Authority
- JP
- Japan
- Prior art keywords
- beckmann rearrangement
- lactam
- temperature
- cycloalkanone oxime
- hydrocarbon
- 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
- Y02P20/10—Process efficiency
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
Abstract
PURPOSE: To eliminate and suppress the foaming in the preparation of ω-lactam by the Beckmann rearrangement of cycloalkanone oxime, effectively, and to improve the production efficiency of the lactam, by adding a slight amount of a hydrocarbon having higher boiling temperature than the temperature of the reaction system.
CONSTITUTION: Cycloalkanone oxime or its derivative (oximes) (e.g. cyclohexanone oxime hydrochloride, α-amino-cyclohexanone oxime hydrochloride, etc.) is subjected to Beckmann rearrangement in the presence of sulfuric acid, chlorosulfonic acid, or sulfur trioxide to obtain the corresponding ω-lactam or its derivative. The above reaction is carried out in the presence of 0.1W10ppm of a hydrocarbon (e.g. n-hexane, n-heptane, etc.) having a boiling point higher than the temperature of said reaction system.
EFFECT: As the lowering of the heat transfer of a heat exchanger is suppressed, the energy efficiency can be improved.
COPYRIGHT: (C)1982,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10513780A JPS5731660A (en) | 1980-08-01 | 1980-08-01 | Beckmann rearrangement of cycloalkanone oxime |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10513780A JPS5731660A (en) | 1980-08-01 | 1980-08-01 | Beckmann rearrangement of cycloalkanone oxime |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5731660A true JPS5731660A (en) | 1982-02-20 |
JPH0159270B2 JPH0159270B2 (en) | 1989-12-15 |
Family
ID=14399356
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10513780A Granted JPS5731660A (en) | 1980-08-01 | 1980-08-01 | Beckmann rearrangement of cycloalkanone oxime |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5731660A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005063388A1 (en) * | 2003-12-25 | 2005-07-14 | Ube Industries, Ltd. | Method for preparing solid acid catalyst and method for producing lactam compound using such catalyst |
-
1980
- 1980-08-01 JP JP10513780A patent/JPS5731660A/en active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005063388A1 (en) * | 2003-12-25 | 2005-07-14 | Ube Industries, Ltd. | Method for preparing solid acid catalyst and method for producing lactam compound using such catalyst |
Also Published As
Publication number | Publication date |
---|---|
JPH0159270B2 (en) | 1989-12-15 |
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