GB1086100A - Improvements in the oxo reaction - Google Patents
Improvements in the oxo reactionInfo
- Publication number
- GB1086100A GB1086100A GB42224/64A GB4222464A GB1086100A GB 1086100 A GB1086100 A GB 1086100A GB 42224/64 A GB42224/64 A GB 42224/64A GB 4222464 A GB4222464 A GB 4222464A GB 1086100 A GB1086100 A GB 1086100A
- Authority
- GB
- United Kingdom
- Prior art keywords
- inert gas
- gas
- hydrogen
- per cent
- amount
- 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)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Aldehydes are prepared by contacting at least one olefinic compound with a mixture of carbon monoxide, hydrogen and a non-condensable inert gas in the presence of a hydroformylation catalyst, the amount of hydrogen being 30-45 mol per cent and the amount of inert gas 5-15 mol per cent based on total of the gas in the reactor. The preferred inert gas is methane or unused gas purged from the reaction mixture, although ethane and nitrogen may also be used. Preferred catalysts are those containing cobalt. Specified olefins are ethylene and propylene. The process is illustrated by reference to flow diagrams (not shown).
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US31720063A | 1963-10-18 | 1963-10-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1086100A true GB1086100A (en) | 1967-10-04 |
Family
ID=23232571
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB42224/64A Expired GB1086100A (en) | 1963-10-18 | 1964-10-16 | Improvements in the oxo reaction |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1086100A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4262142A (en) * | 1979-12-28 | 1981-04-14 | Union Carbide Corporation | Hydroformylation of ethylene with higher olefins |
EP0160249A2 (en) * | 1984-04-28 | 1985-11-06 | Hoechst Aktiengesellschaft | Process for the preparation of aldehydes |
EP4141090A1 (en) | 2021-08-31 | 2023-03-01 | Swedish Biofuels AB | Method for producing motor fuel from ethanol |
-
1964
- 1964-10-16 GB GB42224/64A patent/GB1086100A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4262142A (en) * | 1979-12-28 | 1981-04-14 | Union Carbide Corporation | Hydroformylation of ethylene with higher olefins |
EP0160249A2 (en) * | 1984-04-28 | 1985-11-06 | Hoechst Aktiengesellschaft | Process for the preparation of aldehydes |
EP0160249A3 (en) * | 1984-04-28 | 1987-05-27 | Ruhrchemie Aktiengesellschaft | Process for the preparation of aldehydes |
EP4141090A1 (en) | 2021-08-31 | 2023-03-01 | Swedish Biofuels AB | Method for producing motor fuel from ethanol |
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