GB979673A - Preparation of ester of polyoxyalkylene compounds - Google Patents

Preparation of ester of polyoxyalkylene compounds

Info

Publication number
GB979673A
GB979673A GB4255561A GB4255561A GB979673A GB 979673 A GB979673 A GB 979673A GB 4255561 A GB4255561 A GB 4255561A GB 4255561 A GB4255561 A GB 4255561A GB 979673 A GB979673 A GB 979673A
Authority
GB
United Kingdom
Prior art keywords
acid
polyalkenoxy
compound
alkali metal
metal salt
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
GB4255561A
Inventor
Graham Taylor Pringle
James Herbert Kingsway Rixon
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 GB4255561A priority Critical patent/GB979673A/en
Publication of GB979673A publication Critical patent/GB979673A/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
    • C08G65/02Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/32Polymers modified by chemical after-treatment
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/08Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with the hydroxy or O-metal group of organic compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

An ester of a polyalkenoxy compound, as herein defined, is prepared by reacting the polyalkenoxy compound with a long-chain saturated fatty acid having at least 8 C atoms, in the presence of hypophosphorous acid, or an alkali metal salt thereof, to form a condensate substantially free of colour. The polyalkenoxy compound is one prepared by the reaction of an alkylene oxide, e.g. ethylene oxide or propylene oxide, with a substance containing a reactive hydrogen atom, e.g. an alcohol or amine. The fatty acid may be lauric or stearic acid. The hypophosphorous acid or equivalent amount of alkali metal salt used preferably amounts to between 0.05% and 2% of the total weight of the reactants. An esterification catalyst may be present. An example is given of the esterification of a condensate of 23 mols. ethylene oxide and one mol. of glycerol, with lauric acid, in the presence of hypophosphorous acid, and p-toluene sulphonic acid.ALSO:An ester of a polyalkenoxy compound, as herein defined, is prepared by reacting the polyalkenoxy compound with a saturated long chain fatty acid having at least 8 carbon atoms, in the presence of hypophosphorous acid, or an alkali metal salt thereof, to form a condensate substantially free of colour. The polyalkenoxy compound is one formed by the reaction of an alkylene oxide, e.g. ethylene oxide or propylene oxide, with a substance containing a reactive hydrogen atom, e.g. an alcohol or amine. The fatty acid may be lauric or stearic acid. The hypophosphorous acid or equivalent amount of alkali metal salt used, preferably amounts to between 0.05% and 2% of the total weight of the reactants. An esterification catalyst may be present. An example is given of the esterification of a condensate of 23 mols of ethylene oxide and one mol of glycerol, with lauric acid, in the presence of hypophosphorous acid and p-toluene sulphonic acid.
GB4255561A 1961-11-28 1961-11-28 Preparation of ester of polyoxyalkylene compounds Expired GB979673A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB4255561A GB979673A (en) 1961-11-28 1961-11-28 Preparation of ester of polyoxyalkylene compounds

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB4255561A GB979673A (en) 1961-11-28 1961-11-28 Preparation of ester of polyoxyalkylene compounds

Publications (1)

Publication Number Publication Date
GB979673A true GB979673A (en) 1965-01-06

Family

ID=10424939

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4255561A Expired GB979673A (en) 1961-11-28 1961-11-28 Preparation of ester of polyoxyalkylene compounds

Country Status (1)

Country Link
GB (1) GB979673A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4811084B1 (en) * 1970-07-21 1973-04-10
JPS52100411A (en) * 1976-02-17 1977-08-23 Mitsubishi Monsanto Chem Co Production of ester
DE3516776A1 (en) * 1984-05-14 1985-11-14 Westvaco Corp., New York, N.Y. METHOD FOR PRODUCING COLOPHONIUM PENTAERYTHRITESTER
US4643848A (en) * 1986-02-21 1987-02-17 Westvaco Corporation Modified rosin ester preparation
CN113773196A (en) * 2021-10-08 2021-12-10 上海多纶化工有限公司 Method for synthesizing fatty acid polyglycol ester
CN113861024A (en) * 2021-10-08 2021-12-31 上海多纶化工有限公司 Preparation method of fatty acid polyglycol ester
US11359163B2 (en) * 2018-04-20 2022-06-14 Arkema France Use of hypophosphorous acid for the esterification of free fatty acids

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4811084B1 (en) * 1970-07-21 1973-04-10
JPS52100411A (en) * 1976-02-17 1977-08-23 Mitsubishi Monsanto Chem Co Production of ester
JPS537407B2 (en) * 1976-02-17 1978-03-17
DE3516776A1 (en) * 1984-05-14 1985-11-14 Westvaco Corp., New York, N.Y. METHOD FOR PRODUCING COLOPHONIUM PENTAERYTHRITESTER
US4643848A (en) * 1986-02-21 1987-02-17 Westvaco Corporation Modified rosin ester preparation
US11359163B2 (en) * 2018-04-20 2022-06-14 Arkema France Use of hypophosphorous acid for the esterification of free fatty acids
CN113773196A (en) * 2021-10-08 2021-12-10 上海多纶化工有限公司 Method for synthesizing fatty acid polyglycol ester
CN113861024A (en) * 2021-10-08 2021-12-31 上海多纶化工有限公司 Preparation method of fatty acid polyglycol ester
CN113773196B (en) * 2021-10-08 2024-03-08 上海多纶化工有限公司 Synthesis method of fatty acid polyethylene glycol ester
CN113861024B (en) * 2021-10-08 2024-03-15 上海多纶化工有限公司 Preparation method of fatty acid polyethylene glycol ester

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