GB912034A - Improvements in the preparation of caprolactam - Google Patents
Improvements in the preparation of caprolactamInfo
- Publication number
- GB912034A GB912034A GB10351/60A GB1035160A GB912034A GB 912034 A GB912034 A GB 912034A GB 10351/60 A GB10351/60 A GB 10351/60A GB 1035160 A GB1035160 A GB 1035160A GB 912034 A GB912034 A GB 912034A
- Authority
- GB
- United Kingdom
- Prior art keywords
- nitrosyl
- cyclohexane
- cyclohexyl
- acyl group
- nitrosylation
- 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D201/00—Preparation, separation, purification or stabilisation of unsubstituted lactams
- C07D201/02—Preparation of lactams
- C07D201/08—Preparation of lactams from carboxylic acids or derivatives thereof, e.g. hydroxy carboxylic acids, lactones or nitriles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
- C07D223/02—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D223/06—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D223/08—Oxygen atoms
- C07D223/10—Oxygen atoms attached in position 2
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyrane Compounds (AREA)
Abstract
Caprolactam is prepared by reacting a cyclohexane derivative of formula <FORM:0912034/IV (b)/1> where Y is a substituted or unsubstituted carboxylic acyl group other than an aromatic carboxylic acyl group, with a nitrosylation agent capable of providing NO+ ions in the reaction medium, in the presence of free sulphuric acid. Specified starting materials are those in which Y is -COCH3, -COC(CH3)3, -COCF3, -COCOC6H5, -COCOC6H11 (cyclohexyl) and -C6H11 (cyclohexyl). Specified nitrosylation agents are nitrosyl sulphuric acid, nitrosyl sulphuric anhydride, nitrosyl chloride, nitrosyl bromide, nitrites such as sodium nitrite, alkyl nitrites, and nitrous anhydride. Examples use trimethyl acetyl cyclohexane (obtaining trimethyl acetic acid as by-product), trifluoroacetyl cyclohexane, and dicyclohexylketone. Specifications 904,302 and 904,413 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT560359 | 1959-04-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB912034A true GB912034A (en) | 1962-12-05 |
Family
ID=11120316
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB10351/60A Expired GB912034A (en) | 1959-04-06 | 1960-03-23 | Improvements in the preparation of caprolactam |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB912034A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104529897A (en) * | 2014-12-04 | 2015-04-22 | 湘潭大学 | Method for preparing caprolactam |
-
1960
- 1960-03-23 GB GB10351/60A patent/GB912034A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104529897A (en) * | 2014-12-04 | 2015-04-22 | 湘潭大学 | Method for preparing caprolactam |
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