GB1099712A - Method of producing oxygen-containing organic compounds by the oxo process - Google Patents
Method of producing oxygen-containing organic compounds by the oxo processInfo
- Publication number
- GB1099712A GB1099712A GB2267/65A GB226765A GB1099712A GB 1099712 A GB1099712 A GB 1099712A GB 2267/65 A GB2267/65 A GB 2267/65A GB 226765 A GB226765 A GB 226765A GB 1099712 A GB1099712 A GB 1099712A
- Authority
- GB
- United Kingdom
- Prior art keywords
- oxo process
- alcohols
- hydrogen
- carbon monoxide
- organic compounds
- 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
- C07C45/49—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide
- C07C45/50—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide by oxo-reactions
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Aldehydes and alcohols are prepared by the Oxo process by reacting an olefine, carbon monoxide and hydrogen in the presence of a cobalt containing catalyst under substantially adiabatic conditions with a temperature range 180-350 DEG C. and a pressure range 100-350 atm., the rate of dissolution of the gaseous mixture of carbon monoxide and hydrogen in the liquid olefin or dissolved gaseous olefin being at least 200 normal 1. gas per sec. per 1. liquid. The preferred catalyst is cobalt carbonyl. If sufficient catalyst is used the aldehydes produced by the initial are hydrogenated to alcohols. The reaction is usually completed within 10-45 sec. Decobaltization of the reaction product can be effected in the reactor. Examples relate to the production of butyl alcohol and butyraldehyde from propylene.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2267/65A GB1099712A (en) | 1965-01-19 | 1965-01-19 | Method of producing oxygen-containing organic compounds by the oxo process |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2267/65A GB1099712A (en) | 1965-01-19 | 1965-01-19 | Method of producing oxygen-containing organic compounds by the oxo process |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1099712A true GB1099712A (en) | 1968-01-17 |
Family
ID=9736562
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2267/65A Expired GB1099712A (en) | 1965-01-19 | 1965-01-19 | Method of producing oxygen-containing organic compounds by the oxo process |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1099712A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6270853B1 (en) | 1997-06-20 | 2001-08-07 | Raytheon Company | Electrostatic powder coating of electrically non-conducting substrates |
-
1965
- 1965-01-19 GB GB2267/65A patent/GB1099712A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6270853B1 (en) | 1997-06-20 | 2001-08-07 | Raytheon Company | Electrostatic powder coating of electrically non-conducting substrates |
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