JPS56123963A - Preparation of 2,6-dioxyiminocyclohexanone - Google Patents
Preparation of 2,6-dioxyiminocyclohexanoneInfo
- Publication number
- JPS56123963A JPS56123963A JP11442780A JP11442780A JPS56123963A JP S56123963 A JPS56123963 A JP S56123963A JP 11442780 A JP11442780 A JP 11442780A JP 11442780 A JP11442780 A JP 11442780A JP S56123963 A JPS56123963 A JP S56123963A
- Authority
- JP
- Japan
- Prior art keywords
- cyclohexanone
- acidic catalyst
- dinitrogen trioxide
- cyclohexanol
- titled compound
- 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
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
PURPOSE: To obtain the titled compound useful as a synthetic intermediate for lysine, etc. in high yield and industrially and advantageously, by reacting cyclohexanone with a readily available dinitrogen trioxide or nitrose gas in cyclohexanol in the presence of an acidic catalyst.
CONSTITUTION: Cyclohexanone is reacted with dinitrogen trioxide or nitrose gas in cyclohexanol in the presence of an acidic catalyst, e.g. a mineral acid, at 0W40°C to give the titled compound. The concentration of the acidic catalyst based on the cyclohexanone is preferably 0.1W100mol%, and the amount of the dinitrogen trioxide or nitrose gas is suitably 1W2 times the theoretical one of the cyclohexanone. In the range described above, the conversion of the cyclohexanone reaches about 100% without the necessity for taking the recovery thereof into consideration.
COPYRIGHT: (C)1981,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11442780A JPS56123963A (en) | 1980-08-19 | 1980-08-19 | Preparation of 2,6-dioxyiminocyclohexanone |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11442780A JPS56123963A (en) | 1980-08-19 | 1980-08-19 | Preparation of 2,6-dioxyiminocyclohexanone |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS56123963A true JPS56123963A (en) | 1981-09-29 |
JPS5725541B2 JPS5725541B2 (en) | 1982-05-29 |
Family
ID=14637438
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11442780A Granted JPS56123963A (en) | 1980-08-19 | 1980-08-19 | Preparation of 2,6-dioxyiminocyclohexanone |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS56123963A (en) |
-
1980
- 1980-08-19 JP JP11442780A patent/JPS56123963A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5725541B2 (en) | 1982-05-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPS56123963A (en) | Preparation of 2,6-dioxyiminocyclohexanone | |
JPS5639045A (en) | Recovery of benzylbenzoate | |
JPS5430156A (en) | Synthesis of benzamide derivative | |
JPS579774A (en) | Production of 2-aminobenzothiazole | |
SU1035034A1 (en) | Process for preparing carbamide resin | |
JPS57120570A (en) | Preparation of 1,3-dialkyl-2-imidazolidinone | |
JPS53149912A (en) | Preparation of alkoxyalkylidene compounds | |
JPS53108915A (en) | Preparation of isobutyric acid | |
JPS5772983A (en) | Preparation of 1,2,3,4,6,7,8,9-octahydrophenazine | |
JPS5371010A (en) | Purification of adipic acid ester | |
JPS5466639A (en) | Preparation of monoformylated phenol | |
JPS54106471A (en) | Preparation of 4,5,6,7-tetrahydro-benzimidazoline-2-thione | |
JPS54115376A (en) | Preparation of 5-(4-hydroxyphenyl)-hydantoin | |
JPS55129240A (en) | Preparation of glyoxylic acid | |
JPS5731668A (en) | Preparation of 4,5-dicarbamoylimidazole | |
JPS57102856A (en) | Preparation of oxime compound | |
JPS56164135A (en) | Preparation of 1,2,4-butanetricarboxylic acid | |
JPS5387379A (en) | Preparation of isocyanuric acid triester | |
JPS5337674A (en) | Preparation of pyrazinecarbamoylcarboxylic acid | |
JPS55108856A (en) | Preparation of 1-alkyl-3-methyl-5-pyrazolone | |
JPS5640638A (en) | Preparation of pyruvic acid | |
JPS57188548A (en) | Preparation of beta-chloroalanine | |
JPS5517360A (en) | Preparation of aromatic nitrile | |
JPS5479286A (en) | Preparation of 5-fluoro-orotic acid | |
JPS5334758A (en) | Preparation of alpha-(n-silyl-n-substituted)-carbamoylcarboxylic acid esters |