GB389136A - Improvements relating to the manufacture of aliphatic alcohols - Google Patents
Improvements relating to the manufacture of aliphatic alcoholsInfo
- Publication number
- GB389136A GB389136A GB2548931A GB2548931A GB389136A GB 389136 A GB389136 A GB 389136A GB 2548931 A GB2548931 A GB 2548931A GB 2548931 A GB2548931 A GB 2548931A GB 389136 A GB389136 A GB 389136A
- Authority
- GB
- United Kingdom
- Prior art keywords
- steam
- alkali
- olefines
- alcohol
- mixture
- 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D41/00—Caps, e.g. crown caps or crown seals, i.e. members having parts arranged for engagement with the external periphery of a neck or wall defining a pouring opening or discharge aperture; Protective cap-like covers for closure members, e.g. decorative covers of metal foil or paper
- B65D41/32—Caps or cap-like covers with lines of weakness, tearing-strips, tags, or like opening or removal devices, e.g. to facilitate formation of pouring openings
- B65D41/40—Caps or cap-like covers adapted to be secured in position by permanent deformation of the wall-engaging parts
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Aliphatic alcohols are obtained by the hydration of olefines in presence of basic substances, especially hydroxides of alkali metals. The temperature may be 100-300 DEG C., and atmospheric, reduced, or increased pressure may be employed, but preferably, especially with gaseous olefines, pressure is employed which may be up to 50 atmospheres. If little water is present the product may be an alcoholate, but preferably sufficient water is used to produce alcohols. Liquid olefines may be heated or boiled with alkali hydroxide, preferably in concentrated aqueous solution; or gaseous olefines may be absorbed in circulating aqueous alkali; or a mixture of olefine and steam may be led in contact with aqueous or solid alkali supported on a carrier such as charcoal, silica gel, asbestos, or pumice. The alcohol may be separated by fractional condensation, or the alcohol and steam may be condensed together, the condensate being fractionally distilled with or without an entraining agent. Instead of alkali hydroxides there may be used other basic substances such as calcium or magnesium oxide, which may be used in admixture with one another or with alkali hydroxides. The basic substance may also be used in conjunction with other substances such as thoria or metals such as platinum, gold, silver copper, tungsten, and manganese, or their compounds. In examples (1) a mixture of equal volumes of ethylene and steam is passed into 50 per cent caustic potash solution at 150 DEG C. and 20 atmospheres pressure; (2) a mixture of 1 volume of ethylene and 2 volumes of steam is circulated over pumice impregnated with sodium hydroxide at 200 DEG C. and 30 atmospheres pressure; the vapours are cooled after each treatment or preferably after each ten treatments, the alcohol and steam being condensed together.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2548931A GB389136A (en) | 1931-09-11 | 1931-09-11 | Improvements relating to the manufacture of aliphatic alcohols |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2548931A GB389136A (en) | 1931-09-11 | 1931-09-11 | Improvements relating to the manufacture of aliphatic alcohols |
Publications (1)
Publication Number | Publication Date |
---|---|
GB389136A true GB389136A (en) | 1933-03-13 |
Family
ID=10228520
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2548931A Expired GB389136A (en) | 1931-09-11 | 1931-09-11 | Improvements relating to the manufacture of aliphatic alcohols |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB389136A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3347939A (en) * | 1965-05-21 | 1967-10-17 | Atlantic Refining Co | Conversion of nitroolefins to nitroalcohols |
-
1931
- 1931-09-11 GB GB2548931A patent/GB389136A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3347939A (en) * | 1965-05-21 | 1967-10-17 | Atlantic Refining Co | Conversion of nitroolefins to nitroalcohols |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB404938A (en) | Manufacture of chlorhydrins and ethers thereof | |
GB389136A (en) | Improvements relating to the manufacture of aliphatic alcohols | |
US1986882A (en) | Hydration of olefines | |
US2020673A (en) | Production of oxygen-containing addition products of ethylene | |
GB430764A (en) | Improvements in the manufacture and production of vinyl ethers | |
US2020674A (en) | Manufacture of hydration products of olefines | |
SU138612A1 (en) | The method of obtaining 6-methyl-gentadien-3,5-one-2 | |
GB827450A (en) | Process for the production of epoxy ethers | |
GB368935A (en) | Improvements in the manufacture and production of aliphatic alcohols | |
US1955882A (en) | Process of preparing acetoethyl alcohol | |
Marvel et al. | Di-normal-butyl Ether as a Solvent for the Grignard Reagent | |
GB731917A (en) | Manufacture of 2-ethyl-hexanal-(1) and 2-ethyl-hexanol-(1) | |
SU57892A1 (en) | Method for producing ketones | |
US1206222A (en) | Production of ethylene glycol. | |
GB476898A (en) | Manufacture of esters of salicylic acid | |
GB335631A (en) | Improvements in or relating to the manufacture of oxygenated organic compounds | |
GB370136A (en) | Improvements relating to the conversion of olefines into alcohols | |
ES348644A1 (en) | A procedure for the manufacture of isopropilic alcohol. (Machine-translation by Google Translate, not legally binding) | |
GB451130A (en) | Improved process for direct production of propylene oxide | |
SU95733A1 (en) | Method for producing ethers | |
GB740536A (en) | A process for the manufacture of vinyl chloride | |
GB407722A (en) | Improvements in or relating to the manufacture of hydration products of olefines | |
GB394375A (en) | Improvements in or relating to the hydration of olefines | |
GB813429A (en) | Process for dehydrating ethylene diamine | |
GB644916A (en) | A process for preparing chloral alcoholate or free chloral |