GB1050513A - - Google Patents

Info

Publication number
GB1050513A
GB1050513A GB1050513DA GB1050513A GB 1050513 A GB1050513 A GB 1050513A GB 1050513D A GB1050513D A GB 1050513DA GB 1050513 A GB1050513 A GB 1050513A
Authority
GB
United Kingdom
Prior art keywords
acid
acrylic
sulphonic acid
methacrylic acid
alkali metal
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.)
Active
Application number
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.)
Publication of GB1050513A publication Critical patent/GB1050513A/en
Active legal-status Critical Current

Links

Classifications

    • 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
    • C08F28/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a bond to sulfur or by a heterocyclic ring containing sulfur
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00Sulfonic acids; Halides, esters, or anhydrides thereof

Abstract

1,050,513. Sulpho esters of acrylic and methacrylic acid. DOW CHEMICAL CO. Feb. 20, 1964 [March 1, 1963], No. 7086/64. Heading C2C. [Also in Division C3] An alkali metal salt of a sulpho ester is obtained by heating a mixture of (a) acrylic acid or methacrylic acid, (b) a dry, particulate alkali metal salt of hydroxyethane-sulphonic acid or of hydroxypropanesulphonic acid, (c) a catalyst which is an aromatic or aliphatic sulphonic acid containing from 2 to 12 carbon atoms and mixtures thereof, and (d) an inert organic solvent capable of forming an azeotrope with water, said azeotrope having a boiling-point from 80‹ to 120‹ C., at an esterification reaction temperature of from 80 to 120‹ C. for a period of time sufficient to completely remove water formed by the esterification reaction as a watersolvent azeotrope distillate and recovering the solid sulpho ester alkali metal salt product. The solid starting material is preferably micropulverized and must be free of water. An excess of about 100 mole per cent of a stoichiometric amount of acrylic or methacrylic acid is preferably used. Specified solvents are toluene and benzene. Suitable catalysts are benzene sulphonic acid, lauryl sulphonic acid and toluene sulphonic acid, or a mixture of C 2-12 alkane sulphonic acids. The catalyst is generally used in an amount equal to from about 0À1 to 10À0 weight per cent of the amount of acrylic or methacrylic acid employed. A polymerization inhibitor is preferably employed such as paramethoxy phenol and hydroquinone. The reaction temperature is preferably in the range from 95‹ to 115‹ C. Examples are given in which the sodium salts of 2-sulphoethylacrylate, 2-sulphoethyl methacrylate and 2-sulphopropylacrylate are prepared. The polymers are copolymers derived from the above compounds are useful as flocculating agents and water thickeners (see Division C3). Reference has been directed by the Comptroller to Specification 840,908.
GB1050513D 1963-03-01 Active GB1050513A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US26224563A 1963-03-01 1963-03-01

Publications (1)

Publication Number Publication Date
GB1050513A true GB1050513A (en)

Family

ID=22996771

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1050513D Active GB1050513A (en) 1963-03-01

Country Status (5)

Country Link
BE (1) BE644546A (en)
DE (1) DE1443725A1 (en)
FR (1) FR1383552A (en)
GB (1) GB1050513A (en)
NL (1) NL6401825A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4936214B1 (en) * 1970-01-28 1974-09-28

Also Published As

Publication number Publication date
DE1443725A1 (en) 1969-03-13
FR1383552A (en) 1964-12-24
NL6401825A (en) 1964-09-02
BE644546A (en) 1964-08-28

Similar Documents

Publication Publication Date Title
US3087962A (en) Process of making esters of acrylic and methacrylic acids
GB1050513A (en)
US2375629A (en) Ester of alpha-hydroxy isobutyric acid
US3364183A (en) N, n-bis-acrylamidoacetic compounds, their method of manufacture and their applications
US3759985A (en) Method for preparing salts of sulfoalkyl esters
ES414939A1 (en) Sulfonato-benzyl-malonic acid esters
GB1156573A (en) Method of making diacyl peroxides
GB1242980A (en) A PROCESS OF PREPARING CARBALKOXYALKYL ESTERS OF alpha,beta-UNSATURATED ACIDS
US3176039A (en) Process of preparing carboxylic esters
US3337611A (en) Synthesis of vinyl esters by ester interchange with a molar excess of the carboxylicacid
White 60. A synthesis of methacrylic acid
US3359305A (en) Preparation of sulfo esters of alpha-methylene carboxylic acids
US3141903A (en) Ethylenically unsaturated phenyl salicylate derivatives
Galat A Synthesis of α, β-Unsaturated Amides
ES421284A1 (en) Procedure for the preparation of derivatives of pirrocolinacetic acids. (Machine-translation by Google Translate, not legally binding)
US2959609A (en) Process for preparing vinyl-phosphonic-acid-bis-(beta-chlorethyl)-ester
JPS602287B2 (en) How to remove acetylene compounds
US3712917A (en) Process for separating unsaturated fatty acids
GB1260269A (en) Novel acrylic monomers, their preparation and treatment
US2571639A (en) Phenylation of methacrylic acid
GB1196202A (en) A Process for Producing Ethyleneketals of gamma-Ketocarboxylic Acid Esters
US2552227A (en) Method for preparing esters of 1, 1, 3-alkanetriols
RU2007382C1 (en) Method of methacrylic acid synthesis
JPS537640A (en) Synthesis of diphenylamine derivatives
GB642718A (en) Process for the esterification of fatty acids with low-molecular univalent alcohols