GB1128934A - Improvements in the oxo process - Google Patents
Improvements in the oxo processInfo
- Publication number
- GB1128934A GB1128934A GB52714/65A GB5271465A GB1128934A GB 1128934 A GB1128934 A GB 1128934A GB 52714/65 A GB52714/65 A GB 52714/65A GB 5271465 A GB5271465 A GB 5271465A GB 1128934 A GB1128934 A GB 1128934A
- Authority
- GB
- United Kingdom
- Prior art keywords
- reaction products
- aldehyde
- produced
- boiling point
- oxo process
- 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
1,128,934. Oxo process. EASTMAN KODAK CO. 11 Dec., 1965, No. 52714/65. Heading C2C. An aldehyde is produced by reacting together under pressure an olefine, CO and H 2 in the presence of a cobalt catalyst which is in solution or suspension in a liquid reaction medium, separating the aldehyde and any catalyst from the reaction products, distilling at least a portion of the residual reaction products so as to separate therefrom at least the constituent having the highest boiling point and feeding back the lower boiling point remainder of the residual reaction products or a portion thereof to the liquid reaction medium and continuing the reaction. An example describes the production of butyraldehyde from propylene; alcohols are also produced.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB52714/65A GB1128934A (en) | 1965-12-11 | 1965-12-11 | Improvements in the oxo process |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB52714/65A GB1128934A (en) | 1965-12-11 | 1965-12-11 | Improvements in the oxo process |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1128934A true GB1128934A (en) | 1968-10-02 |
Family
ID=10464999
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB52714/65A Expired GB1128934A (en) | 1965-12-11 | 1965-12-11 | Improvements in the oxo process |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1128934A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4148830A (en) * | 1975-03-07 | 1979-04-10 | Union Carbide Corporation | Hydroformylation of olefins |
US4297239A (en) | 1979-07-16 | 1981-10-27 | Union Carbide Corporation | Hydroformylation catalyst reactivation |
US4374278A (en) * | 1980-02-28 | 1983-02-15 | Union Carbide Corporation | Hydroformylation catalyst reactivation |
-
1965
- 1965-12-11 GB GB52714/65A patent/GB1128934A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4148830A (en) * | 1975-03-07 | 1979-04-10 | Union Carbide Corporation | Hydroformylation of olefins |
US4297239A (en) | 1979-07-16 | 1981-10-27 | Union Carbide Corporation | Hydroformylation catalyst reactivation |
US4374278A (en) * | 1980-02-28 | 1983-02-15 | Union Carbide Corporation | Hydroformylation catalyst reactivation |
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