GB727923A - Preparation of alkali metal alcoholates - Google Patents
Preparation of alkali metal alcoholatesInfo
- Publication number
- GB727923A GB727923A GB28951/52A GB2895152A GB727923A GB 727923 A GB727923 A GB 727923A GB 28951/52 A GB28951/52 A GB 28951/52A GB 2895152 A GB2895152 A GB 2895152A GB 727923 A GB727923 A GB 727923A
- Authority
- GB
- United Kingdom
- Prior art keywords
- oil
- alcohol
- alcohols
- alkali metal
- alcoholates
- 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
- C07C31/00—Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
- C07C31/28—Metal alcoholates
-
- 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
- C07C29/68—Preparation of metal alcoholates
- C07C29/70—Preparation of metal alcoholates by converting hydroxy groups to O-metal groups
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/60—Particles characterised by their size
- C01P2004/61—Micrometer sized, i.e. from 1-100 micrometer
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Liquid Carbonaceous Fuels (AREA)
Abstract
Alkali metal alcoholates suspended in an inert liquid hydrocarbon are obtained by reacting an alkali metal in the form of dispersed particles, having an average size not greater than 100 microns and suspended in an inert hydrocarbon medium with an alcohol. Suitable hydrocarbons are, for example, toluene, xylene, petroleum fractions, straight-run gasoline, kerosene, alkylate, mineral oil, octane, undecane, nonane and substituted naphthalenes. If desired, the alcohol may be premixed with an inert liquid hydrocarbon which may be the same as or different from the hydrocarbon in which the alkali metal is suspended. A dispersing agent may be added to the dispersion of alkali metal. Suitable dispersing agents are fatty acids, activated carbon or clay, and charcoal. The process is suitable for the preparation of alcoholates of alcohols such as methyl, ethyl, propyl, isopropyl, n-butyl, sec.-butyl, tert.-butyl, amyl, hexyl, octyl, decyl, benzyl and xylyl alcohols as well as higher alcohols such as lauryl alcohol, tridecanol, myristyl alcohol, cetyl alcohol, stearyl alcohol, eicosanol and docosanol. It can also be used for forming the alcoholates of unsaturated alcohols such as oleyl, linoleyl, palmitoleyl and eleostearyl alcohols, phytol and ricinoleyl alcohol and of alcohols derived from naturally occurring fats and oils such as sugar cane oil, menhaden oil, cotton seed oil, peanut oil, olive oil, soya oil, tung oil and palm oil. In the examples (a) metallic sodium is dispersed in toluene and treated with ethyl alcohol to give sodium ethylate; (b) metallic sodium is dispersed in toluene and treated with a mixture of alcohols obtained from menhaden oil.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US727923XA | 1952-10-08 | 1952-10-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB727923A true GB727923A (en) | 1955-04-13 |
Family
ID=22109777
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB28951/52A Expired GB727923A (en) | 1952-10-08 | 1952-11-17 | Preparation of alkali metal alcoholates |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB727923A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3345304A (en) * | 1963-11-15 | 1967-10-03 | Rexall Drug Chemical | Neutralization process and apparatus |
US3520940A (en) * | 1967-02-17 | 1970-07-21 | Foot Mineral Co | Process for preparing lithium polyhydric alkoxides |
DE2612642A1 (en) * | 1976-03-25 | 1977-09-29 | Degussa | PROCESS FOR THE PRODUCTION OF SOLUBLE CRYSTAL ALCOHOL-FREE ALKALIMETAL ALCOHOLATES IN INERT SOLVENTS OR SOLVENT MIXTURES |
US4670573A (en) * | 1984-12-17 | 1987-06-02 | Stauffer Chemical Company | Activated preparation of metal alkoxides |
US4748283A (en) * | 1987-02-17 | 1988-05-31 | Lithium Corporation Of America | Hydrocarbon and chlorinated hydrocarbon-soluble magnesium dialkoxides |
EP0749947A1 (en) * | 1995-06-02 | 1996-12-27 | American Cyanamid Company | Continuous process for the manufacture of sodium C4-C8 alkoxide |
-
1952
- 1952-11-17 GB GB28951/52A patent/GB727923A/en not_active Expired
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3345304A (en) * | 1963-11-15 | 1967-10-03 | Rexall Drug Chemical | Neutralization process and apparatus |
US3520940A (en) * | 1967-02-17 | 1970-07-21 | Foot Mineral Co | Process for preparing lithium polyhydric alkoxides |
DE2612642A1 (en) * | 1976-03-25 | 1977-09-29 | Degussa | PROCESS FOR THE PRODUCTION OF SOLUBLE CRYSTAL ALCOHOL-FREE ALKALIMETAL ALCOHOLATES IN INERT SOLVENTS OR SOLVENT MIXTURES |
FR2345417A1 (en) * | 1976-03-25 | 1977-10-21 | Degussa | PROCESS FOR THE PREPARATION OF ALCOHOLATES FROM ALKALINE METALS FREE OF CRYSTALLIZED ALCOHOL, SOLUBLE IN SOLVENTS OR MIXTURES OF INERT SOLVENTS |
US4150244A (en) * | 1976-03-25 | 1979-04-17 | Deutsche Gold- Und Silber-Scheideanstalt Vormals Roessler | Process for the production of crystalline alcohol free alkali metal alcoholates in an inert solvent |
US4670573A (en) * | 1984-12-17 | 1987-06-02 | Stauffer Chemical Company | Activated preparation of metal alkoxides |
US4748283A (en) * | 1987-02-17 | 1988-05-31 | Lithium Corporation Of America | Hydrocarbon and chlorinated hydrocarbon-soluble magnesium dialkoxides |
EP0749947A1 (en) * | 1995-06-02 | 1996-12-27 | American Cyanamid Company | Continuous process for the manufacture of sodium C4-C8 alkoxide |
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