GB1154228A - Process for the Manufacture of Hard Ester Waxes - Google Patents

Process for the Manufacture of Hard Ester Waxes

Info

Publication number
GB1154228A
GB1154228A GB4000266A GB4000266A GB1154228A GB 1154228 A GB1154228 A GB 1154228A GB 4000266 A GB4000266 A GB 4000266A GB 4000266 A GB4000266 A GB 4000266A GB 1154228 A GB1154228 A GB 1154228A
Authority
GB
United Kingdom
Prior art keywords
carbon atoms
acid
alcohol
esters
ether
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
GB4000266A
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.)
Hoechst AG
Original Assignee
Hoechst AG
Farbwerke Hoechst AG
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 Hoechst AG, Farbwerke Hoechst AG filed Critical Hoechst AG
Publication of GB1154228A publication Critical patent/GB1154228A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11CFATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
    • C11C3/00Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
    • C11C3/003Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fatty acids with alcohols
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/24Preparation of carboxylic acid esters by reacting carboxylic acids or derivatives thereof with a carbon-to-oxygen ether bond, e.g. acetal, tetrahydrofuran
    • C07C67/26Preparation of carboxylic acid esters by reacting carboxylic acids or derivatives thereof with a carbon-to-oxygen ether bond, e.g. acetal, tetrahydrofuran with an oxirane ring
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11CFATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
    • C11C3/00Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

1,154,228. Esters. FARBWERKE HOECHST A.G. 7 Sept., 1966 [8 Sept., 1965], No. 40002/66. Heading C2C. Esters containing a hydroxyl group in the #-position to the ester group, and an ether group in the γ-position on the same alcohol side of the ester group are prepared by reacting a glycidyl ether of an aliphatic alcohol of 16 to 30 carbon atoms with either a monocarboxylic acid of 7 to 24 carbon atoms or a polycarboxylic acid having 2 to 12 carbon atoms and 2 to 6 carboxyl groups. The reaction is preferably carried out in the absence of atmospheric oxygen but in the presence of an acid or base catalyst in 0À5 to 4% preferably 2 to 3% proportions by weight of the total mixture, at temperatures between 50 and 300‹ C. more preferably between 80 and 200‹ C. The starting materials are preferably used in equimolar proportions or with an excess of glycidyl ether (about 1 to 3% by weight). The ether is preferably one formed from an alcohol having 16 to 24 carbon atoms, e.g. cetyl, stearyl, behenyl alcohol or mixtures thereof or from the synthetic alcohols obtained from the reaction of ethylene with aluminium triethyl. If the acid is monocarboxylic, it has preferably 7 to 22 carbon atoms; if the acid is polycarboxylic, it has preferably 2 to 8 carbon atoms and 2 to 4 carboxyl groups. The esters thus-formed are hard waxes soluble at room temperature in organic solvents such as balsam, turpentine, gasoline or trichlorethylene to give brilliant films or polishes on evaporation of the solvent.
GB4000266A 1965-09-08 1966-09-07 Process for the Manufacture of Hard Ester Waxes Expired GB1154228A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF47117A DE1257129B (en) 1965-09-08 1965-09-08 Process for the production of hard, soluble ester waxes

Publications (1)

Publication Number Publication Date
GB1154228A true GB1154228A (en) 1969-06-04

Family

ID=7101430

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4000266A Expired GB1154228A (en) 1965-09-08 1966-09-07 Process for the Manufacture of Hard Ester Waxes

Country Status (4)

Country Link
BE (1) BE686598A (en)
DE (1) DE1257129B (en)
GB (1) GB1154228A (en)
NL (1) NL6612516A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3988330A (en) * 1974-10-23 1976-10-26 Emery Industries, Inc. High molecular weight esters of C22+ α-olefin derived acids
US4077991A (en) * 1974-05-02 1978-03-07 The Dow Chemical Company Copolymers of glycidol and glycidyl esters
US4092339A (en) * 1974-05-02 1978-05-30 The Dow Chemical Company Process for making polyglycidyl esters

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4077991A (en) * 1974-05-02 1978-03-07 The Dow Chemical Company Copolymers of glycidol and glycidyl esters
US4092339A (en) * 1974-05-02 1978-05-30 The Dow Chemical Company Process for making polyglycidyl esters
US3988330A (en) * 1974-10-23 1976-10-26 Emery Industries, Inc. High molecular weight esters of C22+ α-olefin derived acids
US4065418A (en) * 1974-10-23 1977-12-27 Emery Industries, Inc. High molecular weight esters of α-alkyl branched monocarboxylic acids

Also Published As

Publication number Publication date
NL6612516A (en) 1967-03-09
DE1257129B (en) 1967-12-28
BE686598A (en) 1967-03-08

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