GB864097A - Polyether derivatives - Google Patents

Polyether derivatives

Info

Publication number
GB864097A
GB864097A GB618958A GB618958A GB864097A GB 864097 A GB864097 A GB 864097A GB 618958 A GB618958 A GB 618958A GB 618958 A GB618958 A GB 618958A GB 864097 A GB864097 A GB 864097A
Authority
GB
United Kingdom
Prior art keywords
alkylene oxides
polyepoxides
polyethers
melt
specified
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
GB618958A
Inventor
Robert Paul Gentles
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 GB618958A priority Critical patent/GB864097A/en
Publication of GB864097A publication Critical patent/GB864097A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H15/00Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
    • C07H15/02Acyclic radicals, not substituted by cyclic structures
    • C07H15/04Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical
    • C07H15/08Polyoxyalkylene derivatives
    • 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
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/48Polyethers
    • C08G18/4895Polyethers prepared from polyepoxy compounds
    • 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
    • C08G65/02Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/26Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
    • C08G65/2603Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen
    • C08G65/2606Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Polyethers (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Abstract

Polyethers are prepared by reacting polyhydroxy compounds with alkylene oxides alone or together with polyepoxides, using dimethyl sulphoxide as reaction medium. The polyhydroxy compounds must melt at temperatures above 120 DEG C. or melt only with decomposition and must be soluble in dimethyl sulphoxide. Suitable compounds are trimethylolethane, pentaerythritol, tetramethylolcyclohexanol, sucrose, a -methyl glucoside and other sugars, mannitol, inositol and quebrachitol. Specified alkylene oxides are ethylene, propylene and butylene oxides. Specified polyepoxides are 1:2-3:4-diepoxybutane, diallyl ether dioxide and 2,6-dioxaspiro-[3,3]-heptane. The reaction may be effected at temperatures of 50 DEG to 150 DEG C. and in the presence of alkaline catalyst. Examples are given in which the reactions are carried out under nitrogen, the catalyst neutralised with adipic acid and then the polyethers bleached with hydrogen peroxide. According to the Provisional Specification, epihalo hydrins such as epichlorhydrin, may be used in place of or in admixture with the alkylene oxides.
GB618958A 1958-02-26 1958-02-26 Polyether derivatives Expired GB864097A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB618958A GB864097A (en) 1958-02-26 1958-02-26 Polyether derivatives

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB618958A GB864097A (en) 1958-02-26 1958-02-26 Polyether derivatives

Publications (1)

Publication Number Publication Date
GB864097A true GB864097A (en) 1961-03-29

Family

ID=9810045

Family Applications (1)

Application Number Title Priority Date Filing Date
GB618958A Expired GB864097A (en) 1958-02-26 1958-02-26 Polyether derivatives

Country Status (1)

Country Link
GB (1) GB864097A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1245385B (en) * 1962-08-28 1967-07-27 Olin Mathieson Process for the preparation of oxyalkylation products of di- or triamino-1, 3, 5-triazines
FR2489344A1 (en) * 1980-09-02 1982-03-05 Texaco Development Corp PROCESS FOR PREPARING HIGH VISCOSITY FLUIDS
FR2489341A1 (en) * 1980-09-02 1982-03-05 Texaco Development Corp POLYOLS MODIFIED BY EPOXY RESINS, PROCESS FOR THEIR PREPARATION AND USE THEREOF FOR THE PREPARATION OF POLYURETHANE FOAMS
EP1403289A1 (en) * 2001-05-14 2004-03-31 Kuraray Co., Ltd. MODIFIED ETHYLENE−VINYL ALCOHOL COPOLYMER AND METHOD FOR THE PRODUCTION THEREOF

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1245385B (en) * 1962-08-28 1967-07-27 Olin Mathieson Process for the preparation of oxyalkylation products of di- or triamino-1, 3, 5-triazines
FR2489344A1 (en) * 1980-09-02 1982-03-05 Texaco Development Corp PROCESS FOR PREPARING HIGH VISCOSITY FLUIDS
FR2489341A1 (en) * 1980-09-02 1982-03-05 Texaco Development Corp POLYOLS MODIFIED BY EPOXY RESINS, PROCESS FOR THEIR PREPARATION AND USE THEREOF FOR THE PREPARATION OF POLYURETHANE FOAMS
EP1403289A1 (en) * 2001-05-14 2004-03-31 Kuraray Co., Ltd. MODIFIED ETHYLENE−VINYL ALCOHOL COPOLYMER AND METHOD FOR THE PRODUCTION THEREOF
EP1403289A4 (en) * 2001-05-14 2004-12-22 Kuraray Co Modified ethylene-vinyl alcohol copolymer and method for the production thereof
US7811646B2 (en) 2001-05-14 2010-10-12 Kuraray Co., Ltd. Modified ethylene-vinyl alcohol copolymer and method for the production thereof
US8329818B2 (en) 2001-05-14 2012-12-11 Kuraray Co., Ltd. Modified ethylene-vinyl alcohol copolymer and method for the production thereof

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