GB934982A - Improvements in and relating to the preparation of ketoximes - Google Patents
Improvements in and relating to the preparation of ketoximesInfo
- Publication number
- GB934982A GB934982A GB5825/60A GB582560A GB934982A GB 934982 A GB934982 A GB 934982A GB 5825/60 A GB5825/60 A GB 5825/60A GB 582560 A GB582560 A GB 582560A GB 934982 A GB934982 A GB 934982A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ketoximes
- reaction
- relating
- preparation
- cyclododecane
- 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.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C249/00—Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C249/04—Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton of oximes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/32—Oximes
- C07C251/34—Oximes with oxygen atoms of oxyimino groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
- C07C251/44—Oximes with oxygen atoms of oxyimino groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with the carbon atom of at least one of the oxyimino groups being part of a ring other than a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D201/00—Preparation, separation, purification or stabilisation of unsubstituted lactams
- C07D201/02—Preparation of lactams
- C07D201/04—Preparation of lactams from or via oximes by Beckmann rearrangement
Abstract
Ketoximes are prepared by reacting saturated hydrocarbons with nitric oxide and chlorine, while irradiating the reactants with light of wavelength 4875 or less, under substantially anhydrous and oxygen-free conditions at a temperature below 15 DEG C. Unsubstituted mononuclear alicyclic hydrocarbons, e.g. cyclohexane and cyclododecane are preferred and the reaction is preferably carried out in the liquid phase, with the hydrocarbon dissolved in a solvent such as carbon tetrachloride, either batchwise or continuously with recirculation. The ketoxime product may be in the form of hydrochloride and may be used to prepare lactams by the Beckmann reaction.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB5825/60A GB934982A (en) | 1960-02-18 | 1960-02-18 | Improvements in and relating to the preparation of ketoximes |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB5825/60A GB934982A (en) | 1960-02-18 | 1960-02-18 | Improvements in and relating to the preparation of ketoximes |
Publications (1)
Publication Number | Publication Date |
---|---|
GB934982A true GB934982A (en) | 1963-08-21 |
Family
ID=9803306
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB5825/60A Expired GB934982A (en) | 1960-02-18 | 1960-02-18 | Improvements in and relating to the preparation of ketoximes |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB934982A (en) |
-
1960
- 1960-02-18 GB GB5825/60A patent/GB934982A/en not_active Expired
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