GB825902A - Condensation and polymerisation agents - Google Patents
Condensation and polymerisation agentsInfo
- Publication number
- GB825902A GB825902A GB12156/58A GB1215658A GB825902A GB 825902 A GB825902 A GB 825902A GB 12156/58 A GB12156/58 A GB 12156/58A GB 1215658 A GB1215658 A GB 1215658A GB 825902 A GB825902 A GB 825902A
- Authority
- GB
- United Kingdom
- Prior art keywords
- carbon
- produced
- alkali metal
- agent
- benzaldehyde
- 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
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/06—Metallic compounds other than hydrides and other than metallo-organic compounds; Boron halide or aluminium halide complexes with organic compounds containing oxygen
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Phenolic Resins Or Amino Resins (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
A condensation and polymerization agent is prepared from an alkali metal and carbon, the ratio of alkali metal to carbon being 1 to 8-64. The agent is decomposed by water to produce hydrogen. The agent may be prepared by heating a mixture of alkali metal and carbon to a temperature of 300-800 DEG C., preferably 600 DEG C., under a layer of carbon. The alkali metal may be sodium or potassium. The carbon may be activated carbon, soot, or graphite. The graphite may be substantially ash-free, finely ground, of particle size 0.5-20m , and of surface area 80 m2/gm., or may be ashrich, coarsely ground, and of surface area 6 m2/gm. The agent may be used in suspension in an inert solvent, e.g. diethyl ether, petroleum ether, hexane, benzene, or xylene.ALSO:A condensation agent comprising a compound of an alkali metal and carbon in which the ratio of alkali metal to carbon is 1 to 8-64 (see Group III) may be used in the production of aldol-like compounds, e.g. diacetone alcohol, or dehydration products thereof, e.g. phorone, depending on the proportion of carbon, its ash content, and state of division, and the dispersion medium. Examples: (a) acetoacetic ester is produced by heating ethyl acetate at a temperature of 90 DEG C. under reflux with petroleum ether and C8K; (b) phorone is produced, together with mesityl oxide, by adding acetone dropwise to diethyl ether containing C8K at room temperature; (c) o -nitrostyrene is produced by interacting benzaldehyde and nitromethane in the cold in the presence of C8K; (d) chalcone is produced by the interaction of acetophenone and benzaldehyde in the cold in the presence of C8K; (e) chloretone is produced by the interaction of acetone and chloroform in the cold in the presence of C8K; (f) malonic ester-benzalacetophenone adduct is produced by interacting the components at room temperature in the presence of C8K; (g) trichloro-butyronitrile is produced by adding a mixture of acrylonitrile and chloroform to a suspension of C8K in diethyl ether at a temperature not exceeding 30 DEG C.; (h) 2-phenyl-1-nitro-ethanol is produced by interacting benzaldehyde and nitromethane in the cold in the presence of C16K. Condensation products of benzaldehyde and malonic acid; and acrylonitrile and nitro-methane may be prepared in a manner similar to that of (f).ALSO:A polymerization agent comprises a compound of an alkali metal and carbon in which the ratio of alkali metal to carbon is 1 to 8-64 (see Group III). An example is given of the polymerization of a -methyl styrene in hexane using a compound of the formula C8K.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE825902X | 1957-04-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB825902A true GB825902A (en) | 1959-12-23 |
Family
ID=6747655
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB12156/58A Expired GB825902A (en) | 1957-04-17 | 1958-04-16 | Condensation and polymerisation agents |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB825902A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3084206A (en) * | 1960-03-23 | 1963-04-02 | British Petroleum Co | Production of hexenes |
US3190937A (en) * | 1960-03-23 | 1965-06-22 | British Petroleum Co | Production of hexenes |
US3278632A (en) * | 1960-12-01 | 1966-10-11 | British Petroleum Co | Catalyst and polymerisation process using said catalyst |
US3325559A (en) * | 1960-03-23 | 1967-06-13 | British Petroleum Co | Production of 4-methylpentene-1 |
US3331884A (en) * | 1960-03-23 | 1967-07-18 | British Petroleum Co | Production of 2-methylpentene-2 |
CN103833540A (en) * | 2013-11-29 | 2014-06-04 | 中山大学 | Beta-substituted chalcone analogue and its preparation method and use in preparation of histone deacetylase inhibitor |
-
1958
- 1958-04-16 GB GB12156/58A patent/GB825902A/en not_active Expired
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3084206A (en) * | 1960-03-23 | 1963-04-02 | British Petroleum Co | Production of hexenes |
US3190937A (en) * | 1960-03-23 | 1965-06-22 | British Petroleum Co | Production of hexenes |
US3325559A (en) * | 1960-03-23 | 1967-06-13 | British Petroleum Co | Production of 4-methylpentene-1 |
US3331884A (en) * | 1960-03-23 | 1967-07-18 | British Petroleum Co | Production of 2-methylpentene-2 |
US3278632A (en) * | 1960-12-01 | 1966-10-11 | British Petroleum Co | Catalyst and polymerisation process using said catalyst |
CN103833540A (en) * | 2013-11-29 | 2014-06-04 | 中山大学 | Beta-substituted chalcone analogue and its preparation method and use in preparation of histone deacetylase inhibitor |
CN103833540B (en) * | 2013-11-29 | 2016-06-08 | 中山大学 | A kind of beta substitution cinnamophenone analogue and its preparation method and the application in preparation NSC 630176 |
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