GB886625A - Process for the manufacture of hexachlorocyclopentene-(2)-one-(1) - Google Patents
Process for the manufacture of hexachlorocyclopentene-(2)-one-(1)Info
- Publication number
- GB886625A GB886625A GB27102/58A GB2710258A GB886625A GB 886625 A GB886625 A GB 886625A GB 27102/58 A GB27102/58 A GB 27102/58A GB 2710258 A GB2710258 A GB 2710258A GB 886625 A GB886625 A GB 886625A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hexachloro
- cyclopentene
- catalyst
- heating
- hexachlorocyclopentene
- 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
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
- C07C49/687—Unsaturated compounds containing a keto groups being part of a ring containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Hexachloro-cyclopentene-3-one-1 or mixtures thereof with hexachloro-cyclopentene-2-one-1 is converted into hexachloro-cyclopenetene-2-one-1 by heating in the presence of an anhydrous aluminium or ferric halide or metallic ion as catalyst at a temperature of from 80 DEG C.-250 DEG C. The rearrangement is preferably carried out by heating at about 120 DEG C. using 0.5%-5% by weight of a catalyst such as ferric chloride. Examples are given. The ketone may be hydrolysed with sodium hydroxide to give perchlorobutadiene carboxylic acid. Hexachloro-cyclopentene-3-one-1 is obtained together with some of the D 2 compound by treating hexachloro-cyclopentadiene with oxygen in the presence of U.V. light.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE886625X | 1957-08-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB886625A true GB886625A (en) | 1962-01-10 |
Family
ID=6833417
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB27102/58A Expired GB886625A (en) | 1957-08-22 | 1958-08-22 | Process for the manufacture of hexachlorocyclopentene-(2)-one-(1) |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB886625A (en) |
-
1958
- 1958-08-22 GB GB27102/58A patent/GB886625A/en not_active Expired
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