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GB825902A - Condensation and polymerisation agents - Google Patents

Condensation and polymerisation agents

Info

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
Application number
GB12156/58A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Honeywell Riedel de Haen AG
Original Assignee
Riedel de Haen AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Riedel de Haen AG filed Critical Riedel de Haen AG
Publication of GB825902A publication Critical patent/GB825902A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F4/00Polymerisation catalysts
    • C08F4/06Metallic 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.
GB12156/58A 1957-04-17 1958-04-16 Condensation and polymerisation agents Expired GB825902A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (7)

* Cited by examiner, † Cited by third party
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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