SE315024B - - Google Patents
Info
- Publication number
- SE315024B SE315024B SE770965A SE770965A SE315024B SE 315024 B SE315024 B SE 315024B SE 770965 A SE770965 A SE 770965A SE 770965 A SE770965 A SE 770965A SE 315024 B SE315024 B SE 315024B
- Authority
- SE
- Sweden
- Prior art keywords
- hydroquinone
- bischloroformate
- resorcinol
- solvent
- isophthaloyl chloride
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/16—Dicarboxylic acids and dihydroxy compounds
- C08G63/18—Dicarboxylic acids and dihydroxy compounds the acids or hydroxy compounds containing carbocyclic rings
- C08G63/19—Hydroxy compounds containing aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyesters Or Polycarbonates (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
In the manufacture of polycarbonates by heating together a dihydric phenol and a bis-haloformate of a dihydric phenol with evolution of hydrogen halide, the reaction is effected in the presence of a solvent which is benzophenone, m-terphenyl, a chlorinated or brominated biphenyl, a chlorinated or brominated diphenyl oxide or a chlorinated or brominated naphthalene. Heating is effected at a temperature from 270 DEG C. to the reflux temperature, possibly in the presence of a tertiary amine as catalyst. The reaction mixture may also include a di-acid halide of an aromatic dicarboxylic acid or a chain-stopper which is a monohydric phenol or an acid halide of a monocarboxylic acid. The dihydric phenols are preferably dihydroxy benzenes, dihydroxy diphenyls, dihydroxy naphthalenes or their halogenated derivatives. They may also be bisphenols in which the radical joining the two hydroxyaryl groups may be one or more radicals selected from alkylene, alkylidene, tertiary amino, ether, carbonyl, sulphide, sulphoxide, sulphore and siloxy radicals and in which the hydroxyaryl groups may be substituted by halo, nitro-, hydrocarbyl or hydrocarbonoxy radicals. The aromatic dicarboxylic acid may be phthalic, isophthalic, terephthalic or a naphthalene dicarboxylic acid or halogen substituted derivatives thereof. At the end of the polymer-forming reaction, the polymer may be precipitated from the solvent by the addition of a non-solvent or, alternatively, the solvent may be removed by spray-drying or evaporation. In examples, polymers are made by reacting: (1) hydroquinone and resorcinol bischloroformate; (2) hydroquinone, hydroquinone bischloroformate and resorcinol bischloroformate; (3) chlorohydroquinone and hydroquinone bischloroformate; (4) hydroquinone and chlorohydroquinone bischloroformate; (5) bisphenol A and bisphenol A bischloroformate; (6) hydroquinone and bisphenol A bischloroformate; (7) hydroquinone, hydroquinone bischloroformate and isophthaloyl chloride by a one- or two-stage process; (8) hydroquinone, hydroquinone bischloroformate and 5 - chloroisophthaloyl chloride; (9) hydroquinone, resorcinol bischloroformate and isophthaloyl chloride; or hydroquinone, resorcinol, hydroquinone bischloroformate and isophthaloyl chloride by a one- or two-stage process; or hydroquinone, hydroquinone bischloroformate, resorcinol bischloroformate and isophthaloyl chloride; or hydroquinone, resorcinol, resorcinol bischloroformate, isophthaloyl chloride and terephthaloyl chloride by a one- or two-stage process. Reference is also made to reacting catechol with the bischloroformate of hydroquinone or resorcinol. Uses.-Films, fibres, electrical insulation or dielectrics, adhesives. Specification 984,524 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US6610860A | 1960-10-31 | 1960-10-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
SE315024B true SE315024B (en) | 1969-09-22 |
Family
ID=22067297
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SE633461A SE308407B (en) | 1960-10-31 | 1961-06-16 | |
SE770965A SE315024B (en) | 1960-10-31 | 1965-06-11 |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SE633461A SE308407B (en) | 1960-10-31 | 1961-06-16 |
Country Status (2)
Country | Link |
---|---|
GB (1) | GB987794A (en) |
SE (2) | SE308407B (en) |
-
1961
- 1961-05-26 GB GB1917661A patent/GB987794A/en not_active Expired
- 1961-06-16 SE SE633461A patent/SE308407B/xx unknown
-
1965
- 1965-06-11 SE SE770965A patent/SE315024B/xx unknown
Also Published As
Publication number | Publication date |
---|---|
GB987794A (en) | 1965-03-31 |
SE308407B (en) | 1969-02-10 |
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