GB871767A - Improvements in or relating to monoesters of 1:2-ethanediol and 1:2-propanediol - Google Patents

Improvements in or relating to monoesters of 1:2-ethanediol and 1:2-propanediol

Info

Publication number
GB871767A
GB871767A GB790859A GB790859A GB871767A GB 871767 A GB871767 A GB 871767A GB 790859 A GB790859 A GB 790859A GB 790859 A GB790859 A GB 790859A GB 871767 A GB871767 A GB 871767A
Authority
GB
United Kingdom
Prior art keywords
ethanediol
monoesters
propanediol
relating
diol
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
GB790859A
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.)
Roehm and Haas GmbH
Original Assignee
Roehm and Haas GmbH
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 Roehm and Haas GmbH filed Critical Roehm and Haas GmbH
Publication of GB871767A publication Critical patent/GB871767A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/02Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
    • C07C69/12Acetic acid esters
    • C07C69/16Acetic acid esters of dihydroxylic compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/02Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
    • C07C69/22Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety
    • C07C69/28Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety esterified with dihydroxylic compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/52Esters of acyclic unsaturated carboxylic acids having the esterified carboxyl group bound to an acyclic carbon atom
    • C07C69/533Monocarboxylic acid esters having only one carbon-to-carbon double bond
    • C07C69/54Acrylic acid esters; Methacrylic acid esters
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F20/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
    • C08F20/02Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
    • C08F20/10Esters
    • C08F20/12Esters of monohydric alcohols or phenols
    • C08F20/16Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
    • C08F20/18Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F20/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
    • C08F20/02Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
    • C08F20/10Esters
    • C08F20/26Esters containing oxygen in addition to the carboxy oxygen

Landscapes

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

Abstract

Mono-esters of 1,2-ethane-diol and/or 1,2-propane-diol with acrylic and/or methacrylic acid are prepared by reacting ethylene oxide and/or propylene oxide with acrylic and/or methacrylic acid at above 30 DEG C. in the presence of ferric chloride, a ferric alcoholate or carboxylate, or chromium tribromide. A polymerization inhibitor such as hydroquinone monomethyl ether may be present. In examples the alkylene oxide is led into a mixture of acid and catalyst.
GB790859A 1958-03-06 1959-03-06 Improvements in or relating to monoesters of 1:2-ethanediol and 1:2-propanediol Expired GB871767A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DER22845A DE1144262B (en) 1958-03-06 1958-03-06 Process for the preparation of AEthane-1, 2-diol and propane-1, 2-diol monoacrylate and monomethacrylate

Publications (1)

Publication Number Publication Date
GB871767A true GB871767A (en) 1961-06-28

Family

ID=7401233

Family Applications (1)

Application Number Title Priority Date Filing Date
GB790859A Expired GB871767A (en) 1958-03-06 1959-03-06 Improvements in or relating to monoesters of 1:2-ethanediol and 1:2-propanediol

Country Status (6)

Country Link
BE (1) BE576414A (en)
CH (1) CH385814A (en)
DE (1) DE1144262B (en)
FR (1) FR1218241A (en)
GB (1) GB871767A (en)
NL (1) NL236750A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1248036B (en) * 1962-12-12 1967-08-24 Basf Ag Process for the preparation of alpha, beta-unsaturated carboxylic acid esters by esterifying the carboxylic acids with alkylene oxides
US3399229A (en) * 1965-04-03 1968-08-27 Cassella Farbwerke Mainkur Ag Process for the production of hydroxyalkyl esters of the alpha, beta-unsaturated carboxylic acids
US3441599A (en) * 1966-05-09 1969-04-29 Mitsubishi Gas Chemical Co Process for preparing hydroxyalkylacrylate or hydroxyalkylmethacrylate
US3441598A (en) * 1966-01-06 1969-04-29 Jefferson Chem Co Inc Acrylate production
DE1911447A1 (en) * 1968-03-09 1970-01-02 Bp Chem Int Ltd Production of carboxylic acid esters
US4069242A (en) 1969-02-06 1978-01-17 The Dow Chemical Company Process for preparation of β-hydroxy esters by reaction of organic carboxylic acids and vicinal epoxides
US4141865A (en) 1977-10-06 1979-02-27 The Dow Chemical Company Catalysts for reaction of carboxylic acids with polyepoxides
US4271312A (en) * 1971-04-07 1981-06-02 Standard Oil Company (Indiana) Suppression of diglycol ether ester in chromium (III) catalyzed ethylene oxide reaction with aromatic carboxylic acids
US4415747A (en) * 1981-09-29 1983-11-15 Union Carbide Corporation Process for making ethylene glycol derivatives

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1287065B (en) * 1963-05-24 1969-01-16 Dow Chemical Co Process for the production of ª ‰ -hydroxyalkyl acrylates and methacrylates by esterification of acrylic acid and methacrylic acid with alkylene oxides
US3340295A (en) * 1963-12-23 1967-09-05 Celanese Corp Process of producing a monoester of an alkylene glycol moiety and a carboxylic acid
US3472775A (en) * 1968-08-14 1969-10-14 Emery Industries Inc Synthetic ester lubricant base fluid containing a polyester thickener

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE515306C (en) * 1926-01-30 1931-10-29 I G Farbenindustrie Akt Ges Process for the preparation of esters
US2484487A (en) * 1948-09-08 1949-10-11 Eastman Kodak Co Process for preparing glycol monoesters of acrylic and alpha-methacrylic acids

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1248036B (en) * 1962-12-12 1967-08-24 Basf Ag Process for the preparation of alpha, beta-unsaturated carboxylic acid esters by esterifying the carboxylic acids with alkylene oxides
US3399229A (en) * 1965-04-03 1968-08-27 Cassella Farbwerke Mainkur Ag Process for the production of hydroxyalkyl esters of the alpha, beta-unsaturated carboxylic acids
US3441598A (en) * 1966-01-06 1969-04-29 Jefferson Chem Co Inc Acrylate production
US3441599A (en) * 1966-05-09 1969-04-29 Mitsubishi Gas Chemical Co Process for preparing hydroxyalkylacrylate or hydroxyalkylmethacrylate
DE1911447A1 (en) * 1968-03-09 1970-01-02 Bp Chem Int Ltd Production of carboxylic acid esters
US4069242A (en) 1969-02-06 1978-01-17 The Dow Chemical Company Process for preparation of β-hydroxy esters by reaction of organic carboxylic acids and vicinal epoxides
US4271312A (en) * 1971-04-07 1981-06-02 Standard Oil Company (Indiana) Suppression of diglycol ether ester in chromium (III) catalyzed ethylene oxide reaction with aromatic carboxylic acids
US4141865A (en) 1977-10-06 1979-02-27 The Dow Chemical Company Catalysts for reaction of carboxylic acids with polyepoxides
US4415747A (en) * 1981-09-29 1983-11-15 Union Carbide Corporation Process for making ethylene glycol derivatives

Also Published As

Publication number Publication date
FR1218241A (en) 1960-05-09
BE576414A (en) 1959-07-01
NL236750A (en)
DE1144262B (en) 1963-02-28
CH385814A (en) 1964-12-31

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