GB633184A - Improvements in and relating to the production of aldehydes - Google Patents
Improvements in and relating to the production of aldehydesInfo
- Publication number
- GB633184A GB633184A GB2740047A GB2740047A GB633184A GB 633184 A GB633184 A GB 633184A GB 2740047 A GB2740047 A GB 2740047A GB 2740047 A GB2740047 A GB 2740047A GB 633184 A GB633184 A GB 633184A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydrogen
- carbon monoxide
- isobutene
- yield
- products
- 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
- C07C27/00—Processes involving the simultaneous production of more than one class of oxygen-containing compounds
- C07C27/20—Processes involving the simultaneous production of more than one class of oxygen-containing compounds by oxo-reaction
- C07C27/22—Processes involving the simultaneous production of more than one class of oxygen-containing compounds by oxo-reaction with the use of catalysts which are specific for this process
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Aldehydes are obtained by reacting an olefine, carbon monoxide and hydrogen at 90 DEG to 180 DEG C. and a superatmospheric pressure of less than 300 atmos., in the presence of metallic cobalt substantially free from other catalytic materials or activators, the molecular ratio of hydrogen to carbon monoxide being from 3 : 1 to 6 : 1, preferably in close proximity to 3 : 1. With ratios below 3 : 1 increasing quantities of paraffin hydrocarbon corresponding to the olefine are produced together with other oxygenated products, and the yield of aldehyde falls. The catalyst may be supported on, e.g. kieselguhr, pumice or alumina or may be fluidized. Metallic cobalt is the preferred catalyst. Olefines instanced are ethylene, propene and their dimers and trimers and especially butenes and their dimers and trimers, such as di-isobutene and tri-butenes. In examples, di-isobutene is reacted with a mixture of hydrogen and carbon monoxide in a molecular ratio of (1) 3 : 1 and (2) 5 : 1, at 130 DEG C., and 250 atmos. pressure, in the presence of metallic cobalt, to give varying quantities of nonaldehyde and unreacted di-isobutene, together with small quantities of octane, condensed products and cobalt compounds. A similar experiment with di-isobutene and a hydrogen: carbon monoxide ratio of 2 : 1 is given to illustrate the fall in yield of nonaldehyde and increased yield of by-products as compared with the reactions of the two examples. In the Provisional Specification it is stated that the molecular ratio of hydrogen to carbon monoxide must be greater than 1 : 1, and that a solid catalyst containing a metal which under the conditions of the reaction forms a carbonyl, may be used.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2740047A GB633184A (en) | 1947-10-13 | 1947-10-13 | Improvements in and relating to the production of aldehydes |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2740047A GB633184A (en) | 1947-10-13 | 1947-10-13 | Improvements in and relating to the production of aldehydes |
Publications (1)
Publication Number | Publication Date |
---|---|
GB633184A true GB633184A (en) | 1949-12-12 |
Family
ID=10258967
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2740047A Expired GB633184A (en) | 1947-10-13 | 1947-10-13 | Improvements in and relating to the production of aldehydes |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB633184A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3008996A (en) * | 1954-04-10 | 1961-11-14 | Montedison Spa | Process for producing aldehydes |
-
1947
- 1947-10-13 GB GB2740047A patent/GB633184A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3008996A (en) * | 1954-04-10 | 1961-11-14 | Montedison Spa | Process for producing aldehydes |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2986588A (en) | Propylene dimerization | |
US2040782A (en) | Manufacture of olefine oxides | |
US2557701A (en) | Catalytic reaction of olefins with carbon monoxide and hydrogen | |
US3879473A (en) | Preparation of ethers from alcohols and olefins catalyzed by iodine | |
TW201402536A (en) | Isononanoic acid proceeding from 2-ethylhexanol, process for preparation thereof and the preparation of conversion products thereof | |
US2448375A (en) | Preparation of carboxylic acids | |
US3527779A (en) | Carboxylic acid preparation | |
US2446132A (en) | Silver catalysts | |
US2380358A (en) | Polymerization of olefins | |
US2526742A (en) | Ketones from secondary alcohols, olefinic compounds, and carbon monoxide | |
US2604495A (en) | Hydrocarbon dehydrogenation in presence of added carbon dioxide | |
US3257459A (en) | Preparation of diethyl ketone in presence of alkaline medium | |
US3898268A (en) | Preparation of unsaturated nitriles using a boron oxide promoter | |
US2497304A (en) | Preparation of carboxylic acid anhydrides | |
GB633184A (en) | Improvements in and relating to the production of aldehydes | |
US2542747A (en) | Olefin reactions | |
Behr et al. | Oligomerization of 1-butene with a homogeneous catalyst system based on allylic nickel complexes | |
US4096188A (en) | Preparation of straight chain aldehydes | |
US2463742A (en) | Ketones | |
US2817669A (en) | Synthesis of organic oxygen-containing compounds | |
US3636156A (en) | Process for the direct production of ketones from olefins | |
US2206376A (en) | Production of hydrocarbons of the gasoline type | |
US4002577A (en) | Copper carbonyl-containing catalytic solutions | |
US3875240A (en) | Synthesis of aldehydes | |
US3004084A (en) | Production of conjugated diolefins |