GB437315A - Improvements in methods of obtaining ketones from alcohols - Google Patents
Improvements in methods of obtaining ketones from alcoholsInfo
- Publication number
- GB437315A GB437315A GB2001134A GB2001134A GB437315A GB 437315 A GB437315 A GB 437315A GB 2001134 A GB2001134 A GB 2001134A GB 2001134 A GB2001134 A GB 2001134A GB 437315 A GB437315 A GB 437315A
- Authority
- GB
- United Kingdom
- Prior art keywords
- solution
- zinc
- catalysts
- alcohols
- ketones
- 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
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
-
- 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
- C07C45/002—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by dehydrogenation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Ketones are prepared by the treatment of alcohols containing more than one carbon atom with catalysts comprising a mixture of easily reducible and difficultly reducible oxides and a metal halide. Such catalysts are described in U.S.A. Specifications 1,625,924, 1,625,927, 1,625,928, and 1,625,929 and preferably contain zinc and chromium oxides and a halide such as zinc chloride. Suitable catalysts may be made (1) by adding zinc oxide to a solution of chromium nitrate zinc chloride and ferric nitrate evaporating to dryness and igniting and then adding some zinc chloride solution; (2) by adding zinc oxide to a solution of cobalt nitrate and then ammonia separating and drying the precipitate and adding zinc chloride solution; (3) by mixing zinc and copper oxides and adding a mixture of cuprous chloride and dextrin solution; (4) by precipitating ferric nitrate solution with ammonia mixing the precipitate with zinc oxide drying and adding ferric chloride. The conversion of the alcohols into ketones may be effected in the presence of water vapour or under reduced pressure. In an example the vapour of 10 per cent aqueous ethyl alcohol is passed at 400 DEG C. over the catalyst prepared by the first method. The vapour is preferably preheated. The reaction temperature may be 250--650 DEG C. The production of acetone from ethyl or isopropyl alcohol, diethyl ketone from propyl alcohol, dipropyl ketone from butyl alcohol, a mixture of diethyl, dipropyl and ethyl propyl ketones from propyl and butyl alcohols and corresponding ketones from secondary butyl, amyl and other alcohols is mentioned. The catalysts may be regenerated when necessary by treatment with air or oxygen at 450--600 DEG C.ALSO:Ketones are prepared by the treatment of alcohols containing more than one carbon atom with catalysts comprising a mixture of easily reducible and difficultly reducible oxides and a metal halide. Such catalysts are described in U.S.A. Specifications 1,625,924, 1,625,927, 1,625,928, and 1,625,929 and preferably contain zinc and chromium oxides and a halide such as zinc chloride. Suitable catalysts may be made (1) by adding zinc oxide to a solution of chromium nitrate, zinc chloride and ferric nitrate evaporating to dryness and igniting and then adding some zinc chloride solution; (2) by adding zinc oxide to a solution of cobalt nitrate and then ammonia separating and drying the precipitate and adding zinc chloride solution; (3) by mixing zinc and copper oxides and adding a mixture of cuprous chloride and dextrin solution; (4) by precipitating ferric nitrate solution with ammonia, mixing the precipitate with zinc oxide, drying and adding ferric chloride. The conversion of the alcohols into ketones may be effected in the presence of water vapour or under reduced pressure. The reaction temperature may be 250--650 DEG C. The production of acetone from isopropyl alcohol, and corresponding ketones from secondary butyl, amyl and other alcohols is mentioned. The catalysts may be regenerated when necessary by treatment with air or oxygen at 450--600 DEG C.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2001134A GB437315A (en) | 1934-07-07 | 1934-07-07 | Improvements in methods of obtaining ketones from alcohols |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2001134A GB437315A (en) | 1934-07-07 | 1934-07-07 | Improvements in methods of obtaining ketones from alcohols |
Publications (1)
Publication Number | Publication Date |
---|---|
GB437315A true GB437315A (en) | 1935-10-28 |
Family
ID=10138867
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2001134A Expired GB437315A (en) | 1934-07-07 | 1934-07-07 | Improvements in methods of obtaining ketones from alcohols |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB437315A (en) |
-
1934
- 1934-07-07 GB GB2001134A patent/GB437315A/en not_active Expired
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