GB693980A - Process for preparing linear polyethers - Google Patents

Process for preparing linear polyethers

Info

Publication number
GB693980A
GB693980A GB1950650A GB1950650A GB693980A GB 693980 A GB693980 A GB 693980A GB 1950650 A GB1950650 A GB 1950650A GB 1950650 A GB1950650 A GB 1950650A GB 693980 A GB693980 A GB 693980A
Authority
GB
United Kingdom
Prior art keywords
diol
disulphonic
ester
specified
molecular proportion
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
GB1950650A
Inventor
Frank Reeder
Eric Richard Wallsgrove
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.)
Akzo Nobel UK PLC
Original Assignee
Courtaulds PLC
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 Courtaulds PLC filed Critical Courtaulds PLC
Priority to GB1950650A priority Critical patent/GB693980A/en
Publication of GB693980A publication Critical patent/GB693980A/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
    • C08G65/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/34Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
    • C08G65/38Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
    • C08G65/40Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols (I) and other compounds (II), e.g. OH-Ar-OH + X-Ar-X, where X is halogen atom, i.e. leaving group
    • C08G65/4093Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols (I) and other compounds (II), e.g. OH-Ar-OH + X-Ar-X, where X is halogen atom, i.e. leaving group characterised by the process or apparatus used
    • 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
    • C08G65/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/34Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
    • C08G65/38Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
    • C08G65/40Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols (I) and other compounds (II), e.g. OH-Ar-OH + X-Ar-X, where X is halogen atom, i.e. leaving group

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyethers (AREA)

Abstract

Linear polyethers having a recurrent unit [Ar-O-R-O], where Ar is an arylene group and R is a divalent linkage group, are made by reacting substantially equimolecular proportions of a dihydric phenol and a disulphonic ester of a diol in presence of an alkali the molecular proportion of which is at least twice the molecular proportion of the disulphonic ester. Specified dihydric phenols are resorcinol, hydroquinone and 3,31- or 4, 41-dihydroxydiphenyl. Specified disulphonic esters are the di-paratoluene sulphonates of ethylene glycol; 1 : 4-bis - (beta - hydroxyethoxy) - benzene; propane - 1,3 - diol; butane - 1,4 - diol; pentane-1,5 - diol; hexane - 1,6 - diol; decane - 1,10-diol; and diethylene glycol. Reaction may be performed in presence of a mixture of dioxane and water. The polymers may be purified by washing with boiling water and boiling hydrochloric acid. They are soluble in meta-cresol and nitrobenzene. Examples are given. Specification 433,452 is referred to.
GB1950650A 1950-08-04 1950-08-04 Process for preparing linear polyethers Expired GB693980A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1950650A GB693980A (en) 1950-08-04 1950-08-04 Process for preparing linear polyethers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1950650A GB693980A (en) 1950-08-04 1950-08-04 Process for preparing linear polyethers

Publications (1)

Publication Number Publication Date
GB693980A true GB693980A (en) 1953-07-08

Family

ID=10130496

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1950650A Expired GB693980A (en) 1950-08-04 1950-08-04 Process for preparing linear polyethers

Country Status (1)

Country Link
GB (1) GB693980A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1259333B (en) * 1964-03-09 1968-01-25 Minnesota Mining & Mfg Process for the preparation of N-alkyl-perfluoroalkanesulphone-amidoalkyl-arylsulphonic acid esters

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1259333B (en) * 1964-03-09 1968-01-25 Minnesota Mining & Mfg Process for the preparation of N-alkyl-perfluoroalkanesulphone-amidoalkyl-arylsulphonic acid esters

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