GB638754A - Improvements in and relating to the synthesis of primary alcohols - Google Patents
Improvements in and relating to the synthesis of primary alcoholsInfo
- Publication number
- GB638754A GB638754A GB1321647A GB1321647A GB638754A GB 638754 A GB638754 A GB 638754A GB 1321647 A GB1321647 A GB 1321647A GB 1321647 A GB1321647 A GB 1321647A GB 638754 A GB638754 A GB 638754A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydrogenation
- atmos
- sio2
- hydrogen
- primary alcohols
- 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
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/16—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxo-reaction combined with reduction
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Primary alcohols are prepared by reaction of an organic compound containing olefinic unsaturation with carbon monoxide and hydrogen in presence of a hydrogenation catalyst at above 300 atmospheres pressure and a temperature above 250 DEG up to 400 DEG C., preferably 325-1500 atmos. and 275-375 DEG C. The molar ratio of olefinic compound: CO : H2 is suitably between 1 : 2 : 2 and 1 : 5 : 20. Suitable olefinic compounds and general conditions of reaction are as specified in Specification 614,010. Copper with aluminium and/or cobalt is preferred as catalyst. Preheating in hydrogen or partial poisoning with sulphur prevents hydrogenation of olefins to alkanes. In examples, propylene is converted to butanols, and ethylene to propanols using catalysts comprising 1Cu : 0.1 Cr : 0.05 Co, 9 Cu : 1 SiO2 or 1 Cu : 1 SiO2 pressure being 1000 atmos. Aldehydes, esters and acids in the products may be reduced to alcohols by hydrogenation. Specification 637,999 also is referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1321647A GB638754A (en) | 1947-05-16 | 1947-05-16 | Improvements in and relating to the synthesis of primary alcohols |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1321647A GB638754A (en) | 1947-05-16 | 1947-05-16 | Improvements in and relating to the synthesis of primary alcohols |
Publications (1)
Publication Number | Publication Date |
---|---|
GB638754A true GB638754A (en) | 1950-06-14 |
Family
ID=10018938
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1321647A Expired GB638754A (en) | 1947-05-16 | 1947-05-16 | Improvements in and relating to the synthesis of primary alcohols |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB638754A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3150188A (en) * | 1960-04-21 | 1964-09-22 | Diamond Alkali Co | Aromatic phosphite catalyst modifiers in the oxo process |
US3274263A (en) * | 1961-08-30 | 1966-09-20 | Shell Oil Co | Process for olefin hydroformylation |
US3290379A (en) * | 1961-09-01 | 1966-12-06 | Diamond Alkali Co | Selective hydroformylation of olefinic compounds |
US3301905A (en) * | 1957-09-28 | 1967-01-31 | Hoechst Ag | Process for oxidizing olefins to aldehydes and ketones |
US3336387A (en) * | 1964-02-28 | 1967-08-15 | Shell Oil Co | Tertiary amine oxides |
US4226845A (en) | 1978-12-06 | 1980-10-07 | S R I International | Water gas shift reaction and in the hydroformylation and hydrohydroxyformylation reactions |
-
1947
- 1947-05-16 GB GB1321647A patent/GB638754A/en not_active Expired
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3301905A (en) * | 1957-09-28 | 1967-01-31 | Hoechst Ag | Process for oxidizing olefins to aldehydes and ketones |
US3150188A (en) * | 1960-04-21 | 1964-09-22 | Diamond Alkali Co | Aromatic phosphite catalyst modifiers in the oxo process |
US3274263A (en) * | 1961-08-30 | 1966-09-20 | Shell Oil Co | Process for olefin hydroformylation |
US3290379A (en) * | 1961-09-01 | 1966-12-06 | Diamond Alkali Co | Selective hydroformylation of olefinic compounds |
US3336387A (en) * | 1964-02-28 | 1967-08-15 | Shell Oil Co | Tertiary amine oxides |
US4226845A (en) | 1978-12-06 | 1980-10-07 | S R I International | Water gas shift reaction and in the hydroformylation and hydrohydroxyformylation reactions |
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