GB1120277A - Preparation of aldehydes by the oxo process - Google Patents
Preparation of aldehydes by the oxo processInfo
- Publication number
- GB1120277A GB1120277A GB30223/65A GB3022365A GB1120277A GB 1120277 A GB1120277 A GB 1120277A GB 30223/65 A GB30223/65 A GB 30223/65A GB 3022365 A GB3022365 A GB 3022365A GB 1120277 A GB1120277 A GB 1120277A
- Authority
- GB
- United Kingdom
- Prior art keywords
- mixture
- propylene
- olefine
- aldehydes
- ethylene
- 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 reacting a mixture of an olefine gas or vapour, carbon monoxide and hydrogen in the presence of a cobalt oxo catalyst soluble in the products. The concentration of the olefine in the mixture to be reacted is from 5 to 20% by volume, and ethyene, if present in the mixture containing an olefine with 3 or 4 C atoms, is in an amount less than 5%, and the temperature of the reaction is at least 75 DEG C., and the pressure of the mixture at least 40 atmospheres. The process is preferably continuous and cobalt oxide on kieselguhr or silica gel is the preferred catalyst. Examples describe the reaction of propylene to form butyraldehyde; of a mixture of propylene and ethylene to form propionaldehyde and n- and is obutyraldehyde; and of ethylene, propylene and butene-1 to form propionaldehyde, n- and iso - butyraldehyde, n - valeraldehyde and 2 - methylbutyraldehyde.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB30223/65A GB1120277A (en) | 1965-07-16 | 1965-07-16 | Preparation of aldehydes by the oxo process |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB30223/65A GB1120277A (en) | 1965-07-16 | 1965-07-16 | Preparation of aldehydes by the oxo process |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1120277A true GB1120277A (en) | 1968-07-17 |
Family
ID=10304240
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB30223/65A Expired GB1120277A (en) | 1965-07-16 | 1965-07-16 | Preparation of aldehydes by the oxo process |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1120277A (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 |
US6265619B1 (en) | 1996-01-17 | 2001-07-24 | Exxon Chemical Patents Inc. | Oxygenates and processes for their manufacture |
WO2015094781A1 (en) | 2013-12-19 | 2015-06-25 | Dow Technology Investments Llc | Hydroformylation process |
-
1965
- 1965-07-16 GB GB30223/65A patent/GB1120277A/en not_active Expired
Cited By (8)
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 |
JPS56100731A (en) * | 1979-12-28 | 1981-08-12 | Union Carbide Corp | Hydroformylation of ethylene form higher olefin |
JPS6254410B2 (en) * | 1979-12-28 | 1987-11-14 | Union Carbide Corp | |
US6265619B1 (en) | 1996-01-17 | 2001-07-24 | Exxon Chemical Patents Inc. | Oxygenates and processes for their manufacture |
WO2015094781A1 (en) | 2013-12-19 | 2015-06-25 | Dow Technology Investments Llc | Hydroformylation process |
JP2016540780A (en) * | 2013-12-19 | 2016-12-28 | ダウ テクノロジー インベストメンツ リミティド ライアビリティー カンパニー | Hydroformylation process |
US9688598B2 (en) | 2013-12-19 | 2017-06-27 | Dow Technology Investments Llc | Hydroformylation process |
JP2020002161A (en) * | 2013-12-19 | 2020-01-09 | ダウ テクノロジー インベストメンツ リミティド ライアビリティー カンパニー | Hydroformylation process |
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