GB665705A - Improvements in synthesis of primary alcohols - Google Patents
Improvements in synthesis of primary alcoholsInfo
- Publication number
- GB665705A GB665705A GB17956/49A GB1795649A GB665705A GB 665705 A GB665705 A GB 665705A GB 17956/49 A GB17956/49 A GB 17956/49A GB 1795649 A GB1795649 A GB 1795649A GB 665705 A GB665705 A GB 665705A
- Authority
- GB
- United Kingdom
- Prior art keywords
- cobalt
- water
- hydrogen
- carbon monoxide
- reacted
- 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 reacting an olefinic hydrocarbon having from 2 to 30 carbon atoms per molecule with carbon monoxide and hydrogen at a temperature in the range of 250 DEG to 400 DEG C. under a pressure of 325-1500 atmospheres, in the presence of from 0.1 to 1.5 parts by weight of water per part of olefine hydrocarbon in the presence of a cobalt salt as catalyst, the cobalt salt being dissolved in at least one of the ingredients of the reaction mixture. Suitable cobalt salts are [Co(CO)4]2, HCo(CO)4, cobalt chloride, cobalt sulphate, cobalt nitrate, cobalt acetate, cobalt propionate, cobalt isobutyrate, cobalt laurate, and cobalt naphthenate. Suitable olefinic hydrocarbons are propylenes, the butenes, butadiene, vinyl cyclohexene, vinyl acetylene, cyclohexene, hexenes, diisobutylene, styrene, tripropylene, tetrapropylene, triisobutylene and tetra-isobutylene. Other inert gaseous or liquid diluents may be employed in addition to water, e.g. benzene and dioxane. In the examples: (a) diisobutylene is reacted in the presence of water and cobalt acetate with a mixture of hydrogen, carbon monoxide and carbon dioxide to give 3,5,5-trimethyl-hexanol-1; (b) propylene is reacted with hydrogen and carbon monoxide in the presence of cobalt acetate and water to p give n-butanol, isobutanol and some butyl formate; (c) vinylcyclohexene is reacted with carbon monoxide and hydrogen in the presence of cobalt acetate and water to give monohydric and dihydric alcohols; (d) tetraisobutylene is reacted with carbon monoxide and hydrogen in the presence of water and cobalt acetate; and (e) ethylene is reacted with carbon monoxide and hydrogen in the presence of cobalt acetate and water to give methyl pentanol-1. Specifications 631,316, 637,999, 638,754 and 662,706 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US665705XA | 1948-07-24 | 1948-07-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB665705A true GB665705A (en) | 1952-01-30 |
Family
ID=22070330
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB17956/49A Expired GB665705A (en) | 1948-07-24 | 1949-07-07 | Improvements in synthesis of primary alcohols |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB665705A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2738370A (en) * | 1951-07-11 | 1956-03-13 | Exxon Research Engineering Co | Preparation of alicyclic glycols |
DE1028555B (en) * | 1954-04-02 | 1958-04-24 | Exxon Research Engineering Co | Process for the production of aldehydes by the oxo synthesis |
US3095451A (en) * | 1956-12-18 | 1963-06-25 | Ruhrchemie Ag | Catalytic addition of carbon monoxide and hydrogen to olefinic compounds |
US4267383A (en) * | 1979-05-04 | 1981-05-12 | Celanese Corporation | Hydrocarbonylation |
US4482748A (en) * | 1967-05-29 | 1984-11-13 | Celanese Corporation | Hydrocarbonylation |
-
1949
- 1949-07-07 GB GB17956/49A patent/GB665705A/en not_active Expired
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2738370A (en) * | 1951-07-11 | 1956-03-13 | Exxon Research Engineering Co | Preparation of alicyclic glycols |
DE1028555B (en) * | 1954-04-02 | 1958-04-24 | Exxon Research Engineering Co | Process for the production of aldehydes by the oxo synthesis |
US3095451A (en) * | 1956-12-18 | 1963-06-25 | Ruhrchemie Ag | Catalytic addition of carbon monoxide and hydrogen to olefinic compounds |
US4482748A (en) * | 1967-05-29 | 1984-11-13 | Celanese Corporation | Hydrocarbonylation |
US4267383A (en) * | 1979-05-04 | 1981-05-12 | Celanese Corporation | Hydrocarbonylation |
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