GB410816A - Improvements in or relating to the manufacture of hydration products of olefines - Google Patents
Improvements in or relating to the manufacture of hydration products of olefinesInfo
- Publication number
- GB410816A GB410816A GB32635/32A GB3263532A GB410816A GB 410816 A GB410816 A GB 410816A GB 32635/32 A GB32635/32 A GB 32635/32A GB 3263532 A GB3263532 A GB 3263532A GB 410816 A GB410816 A GB 410816A
- Authority
- GB
- United Kingdom
- Prior art keywords
- absorption
- alcohol
- benzene
- sulphuric acid
- product
- 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
- C07C29/03—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2
- C07C29/04—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2 by hydration of carbon-to-carbon double bonds
- C07C29/05—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2 by hydration of carbon-to-carbon double bonds with formation of absorption products in mineral acids and their hydrolysis
- C07C29/06—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2 by hydration of carbon-to-carbon double bonds with formation of absorption products in mineral acids and their hydrolysis the acid being sulfuric acid
-
- 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
- C07C29/74—Separation; Purification; Use of additives, e.g. for stabilisation
- C07C29/76—Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment
- C07C29/86—Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment by liquid-liquid treatment
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Environmental & Geological Engineering (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Geology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The alcohols or ethers produced by hydrolysis of the products obtained by absorption of olefines in strong acids such as sulphuric or phosphoric acid, are separated by adding an organic liquid acting to extract the alcohol or ether or to entrain the alcohol or ether and if desired the water in a distillation process. Suitable liquids are benzene, decahydronaphthalene, tetrachlorethane, chlorbenzene, and petroleum fractions of boiling-point between 80 and 150 DEG C. When the added liquid is to be used as a solvent, chlorbenzene, hydrogenated naphthalenes, or tetrachlorethane are suitable in the case of ethyl alcohol, while for entraining ethyl alcohol, benzene, trichlorethylene n-hexane, cyclohexane, and chloroform are suitable, while diethyl ether may be entrained by n-pentane. When an entraining agent is employed, it may be brought into contact with the alcoholic liquor in liquid or vapour form, and the solvent layer of the distillate may be returned to the distillation apparatus. A salt such as ammonium sulphate may be added to the alcoholic liquor before extraction of the alcohol. In examples (1) the product of the absorption of ethylene in sulphuric acid is diluted with ammonium sulphate solution and extracted with chlorbenzene in two stages; (2) the hydrolysis product of the absorption of isobutylene in sulphuric acid is extracted with benzene in three stages; an aqueous solution of the alcohol may be obtained by treating the extract with water; (3) the hydrolyzed product of the absorption of propylene in sulphuric acid is distilled with n-hexane; (4) the hydrolyzed product of the absorption of ethylene in sulphuric acid is distilled with cyclohexane or benzene; (5) the same hydrolysis product is passed down a column, the top of which is maintained at 70 DEG C. and n-hexane vapour is passed up the column. Specification 389,134 is referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB32635/32A GB410816A (en) | 1932-11-18 | 1932-11-18 | Improvements in or relating to the manufacture of hydration products of olefines |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB32635/32A GB410816A (en) | 1932-11-18 | 1932-11-18 | Improvements in or relating to the manufacture of hydration products of olefines |
Publications (1)
Publication Number | Publication Date |
---|---|
GB410816A true GB410816A (en) | 1934-05-18 |
Family
ID=10341699
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB32635/32A Expired GB410816A (en) | 1932-11-18 | 1932-11-18 | Improvements in or relating to the manufacture of hydration products of olefines |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB410816A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2597009A (en) * | 1948-05-28 | 1952-05-20 | Kellogg M W Co | Dehydration of alcohols |
US2695867A (en) * | 1950-01-27 | 1954-11-30 | Stone & Webster Eng Corp | Combination extraction and distillation process |
US4547354A (en) * | 1983-10-31 | 1985-10-15 | Atlantic Richfield Company | Process for preparing hydrogen peroxide |
-
1932
- 1932-11-18 GB GB32635/32A patent/GB410816A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2597009A (en) * | 1948-05-28 | 1952-05-20 | Kellogg M W Co | Dehydration of alcohols |
US2695867A (en) * | 1950-01-27 | 1954-11-30 | Stone & Webster Eng Corp | Combination extraction and distillation process |
US4547354A (en) * | 1983-10-31 | 1985-10-15 | Atlantic Richfield Company | Process for preparing hydrogen peroxide |
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