GB644468A - Improvements in or relating to the production of new resinous polyesters - Google Patents

Improvements in or relating to the production of new resinous polyesters

Info

Publication number
GB644468A
GB644468A GB11748A GB11748A GB644468A GB 644468 A GB644468 A GB 644468A GB 11748 A GB11748 A GB 11748A GB 11748 A GB11748 A GB 11748A GB 644468 A GB644468 A GB 644468A
Authority
GB
United Kingdom
Prior art keywords
dichloride
benzene
dichlorophenoxyphosphoryl
aryloxyphosphoryl
dihydroxydiphenyl
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
GB11748A
Inventor
Henryk Zenftman
Andrew Mclean
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB11748A priority Critical patent/GB644468A/en
Priority to BE485671A priority patent/BE485671A/en
Priority to FR985505D priority patent/FR985505A/en
Priority to DE1948818696D priority patent/DE818696C/en
Priority to CH282638D priority patent/CH282638A/en
Priority to CH277666D priority patent/CH277666A/en
Publication of GB644468A publication Critical patent/GB644468A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G79/00Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule
    • C08G79/02Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule a linkage containing phosphorus
    • C08G79/04Phosphorus linked to oxygen or to oxygen and carbon

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)

Abstract

Synthetic resins are prepared by condensing an aryloxyphosphoryl dichloride with a dihydric phenol, the hydroxyl groups of which are attached to non-adjacent carbon atoms. Catalysts, e.g. tin, calcium chloride, boron trifluoride, or zinc or aluminium chloride may be present, or the reaction may be performed in a solvent, e.g. ether, benzene or chloroform with, if desired, an acid acceptor, e.g. a tertiary amine such as pyridine, present. Specified phenols are hydroquinone, resorcinol, chlorinated hydroquinone, dihydroxy naphthalene, 2,21- or 4,41-dihydroxydiphenyl and chlorinated dihydroxydiphenyl. Specified aryloxyphosphoryl dichlorides are phenoxyphosphoryl dichloride; p - chlorophenoxyphosphoryl dichloride; o - chlorophenoxyphosphory dichloride; 2,4-dichlorophenoxyphosphoryl dichloride; 2,4,6-trichlorophenoxyphosphoryl dichloride; 2,4-dibromophenoxyphosphoryl dichloride; o-methylphenoxyphosphoryl dichloride; 2-methyl-4,6-dichlorophenoxyphosphoryl dichloride. They may be prepared by the method of Specification 644,467, [Group IV (b)]. Reaction may be effected by heating progressively from 100-180 DEG C. to 190-240 DEG C. Preferably the mixture is stirred. An inert atmosphere may be maintained. The products are soluble in dioxane, chloroform, benzene-alcohol mixtures, benzene, toluene, or mixtures of butyl or amyl acetate and aromatic hydrocarbons containing minor proportions of aliphatic alcohols. Some of these are soluble in butyl acetate, ethyl acetate, and acetone. They may be purified by dissolving them in benzene and precipitating with ether and by washing with sodium carbonate. They may be rendered infusible by heating with metallic oxides, e.g. litharge. They are compatible with nitrocellulose, ethyl cellulose and polyvinyl chloride. A number of examples are given of the preparation of resins according to the invention.
GB11748A 1948-01-02 1948-01-02 Improvements in or relating to the production of new resinous polyesters Expired GB644468A (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
GB11748A GB644468A (en) 1948-01-02 1948-01-02 Improvements in or relating to the production of new resinous polyesters
BE485671A BE485671A (en) 1948-01-02 1948-11-05 Improvements in the production of new resinous polyesters
FR985505D FR985505A (en) 1948-01-02 1948-11-05 Manufacture of new resinous polyesters
DE1948818696D DE818696C (en) 1948-01-02 1948-11-07 Process for the production of resinous polyesters
CH282638D CH282638A (en) 1948-01-02 1948-12-31 Method of making a new resinous material.
CH277666D CH277666A (en) 1948-01-02 1948-12-31 Method of making a new resinous material.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB11748A GB644468A (en) 1948-01-02 1948-01-02 Improvements in or relating to the production of new resinous polyesters

Publications (1)

Publication Number Publication Date
GB644468A true GB644468A (en) 1950-10-11

Family

ID=9698706

Family Applications (1)

Application Number Title Priority Date Filing Date
GB11748A Expired GB644468A (en) 1948-01-02 1948-01-02 Improvements in or relating to the production of new resinous polyesters

Country Status (5)

Country Link
BE (1) BE485671A (en)
CH (1) CH277666A (en)
DE (1) DE818696C (en)
FR (1) FR985505A (en)
GB (1) GB644468A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE905368C (en) * 1950-09-09 1954-03-01 Basf Ag Process for the production of neutral phosphoric acid alkyl esters
US2716100A (en) * 1952-09-10 1955-08-23 Eastman Kodak Co Resinous, linear polymeric chloroalkanephosphonates
US3008951A (en) * 1952-06-17 1961-11-14 Leo Ab Anti-enzymatic substances

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL179175B (en) * 1952-06-17 Rca Corp FREQUENCY CONTROLLED OSCILLATOR.
BE533446A (en) * 1953-11-18
US2964552A (en) * 1956-08-31 1960-12-13 Leo Ab Adrenocorticotropic action-retarding and anti-enzymatic substances

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE905368C (en) * 1950-09-09 1954-03-01 Basf Ag Process for the production of neutral phosphoric acid alkyl esters
US3008951A (en) * 1952-06-17 1961-11-14 Leo Ab Anti-enzymatic substances
US2716100A (en) * 1952-09-10 1955-08-23 Eastman Kodak Co Resinous, linear polymeric chloroalkanephosphonates

Also Published As

Publication number Publication date
BE485671A (en) 1949-05-05
DE818696C (en) 1951-10-25
FR985505A (en) 1951-07-19
CH277666A (en) 1952-01-03

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