GB1039377A - Improvements in polymeric glycidyl polyethers and their preparation - Google Patents

Improvements in polymeric glycidyl polyethers and their preparation

Info

Publication number
GB1039377A
GB1039377A GB1934263A GB1934263A GB1039377A GB 1039377 A GB1039377 A GB 1039377A GB 1934263 A GB1934263 A GB 1934263A GB 1934263 A GB1934263 A GB 1934263A GB 1039377 A GB1039377 A GB 1039377A
Authority
GB
United Kingdom
Prior art keywords
phenol
epihalohydrin
prepared
dihydric phenol
mols
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
GB1934263A
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.)
Celanese Coatings Co Inc
Original Assignee
Devoe and Raynolds Co Inc
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 Devoe and Raynolds Co Inc filed Critical Devoe and Raynolds Co Inc
Publication of GB1039377A publication Critical patent/GB1039377A/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
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/02Polycondensates containing more than one epoxy group per molecule
    • C08G59/04Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof
    • C08G59/06Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols
    • C08G59/063Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols with epihalohydrins

Landscapes

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

Abstract

Phenol polyether alcohols of the formula HOR(OCH2CHOHCH2OR)zOCH2CHOH CH2OROH wherein R is the divalent radical of a dihydric phenol R(OH)2 and z is 0 or an integer are prepared by reacting z+2 mols. of the dihydric phenol with z+1 mols. of epichlorohydrin in the presence of caustic soda. In examples phenol polyether alcohols in which z=0, 1, 2 and 3 are prepared from bisphenol A and a phenol polyether alcohol in which z=2 is prepared from resorcinol.ALSO:Polymeric glycidyl polyethers are prepared by reacting (1) a complex phenol polyether alcohol of formula HOR(OCH2CHOHCH2OR)zOCH2CHOHCH2OROH wherein R represents the divalent radical from a dihydric phenol R(OH)2 and z is O or an integer up to 10, with (2) a molar excess of an epihalohydrin in the presence of a caustic alkali as a dehydrohalogenating agent, the number of mols. of epihalohydrin being x(z+2), wherein x is a number from 1.5 to 10. The complex phenols used are the reaction products of a dihydric phenol (in excess) and either an epihalohydrin or a diglycidyl ether of a dihydric phenol. The complex phenol and epihalohydrin may be condensed in the presence of an alkaline material before dehydrohalogenation with an alkali metal hydroxide or both reactions may be performed in one step in the presence of an alkali metal hydroxide.
GB1934263A 1962-06-06 1963-05-15 Improvements in polymeric glycidyl polyethers and their preparation Expired GB1039377A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US20030162A 1962-06-06 1962-06-06

Publications (1)

Publication Number Publication Date
GB1039377A true GB1039377A (en) 1966-08-17

Family

ID=22741133

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1934263A Expired GB1039377A (en) 1962-06-06 1963-05-15 Improvements in polymeric glycidyl polyethers and their preparation

Country Status (4)

Country Link
BE (1) BE633173A (en)
CH (1) CH465885A (en)
GB (1) GB1039377A (en)
NL (1) NL293699A (en)

Also Published As

Publication number Publication date
CH465885A (en) 1968-11-30
BE633173A (en)
DE1493582A1 (en) 1972-04-13
DE1493582B2 (en) 1973-01-04
NL293699A (en)

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