GB1207561A - Oxo process - Google Patents
Oxo processInfo
- Publication number
- GB1207561A GB1207561A GB0396/68A GB139668A GB1207561A GB 1207561 A GB1207561 A GB 1207561A GB 0396/68 A GB0396/68 A GB 0396/68A GB 139668 A GB139668 A GB 139668A GB 1207561 A GB1207561 A GB 1207561A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ligand
- rhodium
- neutral
- carbonyl
- treated
- 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
1,207,561. Oxo process. BRITISH PETROLEUM CO. Ltd. 6 Dec., 1968 [10 Jan., 1968], No. 1396/68. Heading C2C. Olefins are hydroformylated with CO and H 2 at elevated temperatures in the presence of a zerovalent rhodium species containing at least one carbonyl ligand and also containing and/or in the presence of at least one neutral ligand containing an atom of a Group V B or VIB element which has a single pair of electrons available for donation, e.g. P, N, As, Sb or S. Suitable neutral ligands include phosphines, phosphites, arsines, stibines, pyridines, amines and sulphoxides. The catalyst may be formed in situ by adding rhodium carbonyl and the neutral ligand to the reaction mixture. Alternatively a suspension of rhodium hydroxide may be treated with CO and the resulting solid treated with the ligand in a reaction solvent medium. Suitable solvents include alcohols, hydrocarbons and amides. Examples prepare n - heptaldehyde and 2 - methylhexaldehyde from hexene - 1 in heptane and n - heptanol and 2 - methylhexanol using n - octanol as solvent.
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0396/68A GB1207561A (en) | 1968-01-10 | 1968-01-10 | Oxo process |
NL6818254A NL6818254A (en) | 1968-01-10 | 1968-12-19 | |
FR1600074D FR1600074A (en) | 1968-01-10 | 1968-12-30 | |
DE19691901145 DE1901145A1 (en) | 1968-01-10 | 1969-01-10 | Process for the hydroformylation of olefins |
BE726744D BE726744A (en) | 1968-01-10 | 1969-01-10 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0396/68A GB1207561A (en) | 1968-01-10 | 1968-01-10 | Oxo process |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1207561A true GB1207561A (en) | 1970-10-07 |
Family
ID=9721276
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB0396/68A Expired GB1207561A (en) | 1968-01-10 | 1968-01-10 | Oxo process |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE726744A (en) |
DE (1) | DE1901145A1 (en) |
FR (1) | FR1600074A (en) |
GB (1) | GB1207561A (en) |
NL (1) | NL6818254A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2424526A1 (en) * | 1974-05-21 | 1975-12-04 | Exxon Research Engineering Co | Hydroformylation of alpha olefins to aldehydes - using zero valent rhodium complexes as oxidn. catalyst |
US3946082A (en) * | 1972-03-24 | 1976-03-23 | Exxon Research & Engineering Co. | Preparation of zerovalent phosphine substituted rhodium compounds and their use in the selective carbonylation of olefins |
US4260828A (en) * | 1980-04-16 | 1981-04-07 | Union Carbide Corporation | Hydroformylation process |
US4496768A (en) * | 1982-06-11 | 1985-01-29 | Davy Mckee Limited | Process for the production of aldehydes by hydroformylation of alpha-olefins |
US4496769A (en) * | 1982-06-11 | 1985-01-29 | Davy Mckee (London) Limited | Process for the preparation of aldehydes by hydroformylation of olefins |
-
1968
- 1968-01-10 GB GB0396/68A patent/GB1207561A/en not_active Expired
- 1968-12-19 NL NL6818254A patent/NL6818254A/xx unknown
- 1968-12-30 FR FR1600074D patent/FR1600074A/fr not_active Expired
-
1969
- 1969-01-10 BE BE726744D patent/BE726744A/xx unknown
- 1969-01-10 DE DE19691901145 patent/DE1901145A1/en active Pending
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3946082A (en) * | 1972-03-24 | 1976-03-23 | Exxon Research & Engineering Co. | Preparation of zerovalent phosphine substituted rhodium compounds and their use in the selective carbonylation of olefins |
DE2424526A1 (en) * | 1974-05-21 | 1975-12-04 | Exxon Research Engineering Co | Hydroformylation of alpha olefins to aldehydes - using zero valent rhodium complexes as oxidn. catalyst |
DE2463148C2 (en) * | 1974-05-21 | 1986-04-30 | Exxon Research And Engineering Co., Florham Park, N.J. | Process for the production of aldehydes |
US4260828A (en) * | 1980-04-16 | 1981-04-07 | Union Carbide Corporation | Hydroformylation process |
US4496768A (en) * | 1982-06-11 | 1985-01-29 | Davy Mckee Limited | Process for the production of aldehydes by hydroformylation of alpha-olefins |
US4496769A (en) * | 1982-06-11 | 1985-01-29 | Davy Mckee (London) Limited | Process for the preparation of aldehydes by hydroformylation of olefins |
Also Published As
Publication number | Publication date |
---|---|
BE726744A (en) | 1969-07-10 |
DE1901145A1 (en) | 1969-08-28 |
FR1600074A (en) | 1970-07-20 |
NL6818254A (en) | 1969-07-14 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PLNP | Patent lapsed through nonpayment of renewal fees |