GB900506A - Esters containing epoxide groups, their production and their uses - Google Patents

Esters containing epoxide groups, their production and their uses

Info

Publication number
GB900506A
GB900506A GB4377459A GB4377459A GB900506A GB 900506 A GB900506 A GB 900506A GB 4377459 A GB4377459 A GB 4377459A GB 4377459 A GB4377459 A GB 4377459A GB 900506 A GB900506 A GB 900506A
Authority
GB
United Kingdom
Prior art keywords
anhydride
compounds
mono
esters
acid
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
GB4377459A
Inventor
Reginald Francis Webb
Eric Johnston
Bernard Peter Stark
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.)
BASF Schweiz AG
Ciba ARL Ltd
Original Assignee
Ciba AG
Ciba ARL 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 Ciba AG, Ciba ARL Ltd filed Critical Ciba AG
Priority to GB4377459A priority Critical patent/GB900506A/en
Publication of GB900506A publication Critical patent/GB900506A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D303/00Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
    • C07D303/02Compounds containing oxirane rings
    • C07D303/12Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
    • C07D303/16Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by esterified hydroxyl radicals
    • 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
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/20Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
    • C08G59/22Di-epoxy compounds
    • C08G59/24Di-epoxy compounds carbocyclic

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Epoxy Resins (AREA)

Abstract

Hardenable compositions comprise esters of the formula <FORM:0900506/IV(a)/1> and one or more hardeners therefor, such as amines or amides, e.g. mono-, di- and tributylamine, p-phenylenediamine, bis(p-aminophenyl)methane, ethylenediamine, N:N-diethylethylenediamine, diethylenetriamine, tetra(hydroxyethyl)-diethylenetriamine, triethylenetetramine, tetraethylenepentamine, trimethylamine, diethylamine, triethanolamine, Mannich bases, piperidine, guanidine, phenyl guanidine and diphenyl guanidine, dicyandiamide, aniline-formaldehyde resins, polymers of amino-styrenes, polyamides, e.g. from aliphatic polyamines and di- or tri-merised unsaturated fatty acids, isocyanates, isothiocyanates, resorcinol, hydroquinone, bis(4-hydroxyphenyl)-dimethylmethane and quinone, phenol-aldehyde resins, oil-modified phenolaldehyde resins, reaction products of aluminium alkoxides or phenolates with tautomeric reacting compounds of the acetoacetic ester type, Friedel-Crafts catalysts, e.g. AlCl3, SbCl5, SnCl4, ZnCl2, BF3 and the complexes with organic compounds, and phosphoric acid. Preferred hardeners are polybasic carboxylic acids and their anhydrides, e.g. phthalic anhydride, methylenedimethylenetetrahydrophthalic anhydride, dodecenyl succinic anhydrides hexahydrophthalic anhydride, hexachloroendomethylenetetrahydrophthalic anhydride or endomethylenetetrahydrophthalic anhydride or their mixtures, or maleic or succinic anhydrides. Accelerators such as tertiary amines and polyhydroxy compounds such as hexanetriol and glycerol may be present in some cases. The hardenable mixtures may contain a proportion of the epoxy esters in which one or both of the epoxy groups are hydrolysed to hydroxyl groups, and/or other polyhydroxy compounds such as hexanetriol. Other epoxides, e.g. mono- or polyglycidyl ethers of mono- or polyalcohols such as butyl alcohol, butane-1:4-diol or glycerine, or mono or polyphenols, e.g. resorcinol, bis(4-hydroxyphenol) dimethylmethane or Novolaks; polyglycidyl esters of polycarboxylic esters, such as phthalic acid, or aminopolyepoxides obtained by dehydrohalogenation of products from epichlorhydrin and amines such as n-butylamine, aniline or 4:41-di-(monomethylamine)-diphenylmethane, may also be present. The compositions may also contain asphalt, bitumen, glass fibres, mica, quartz, powder, cellulose, kaolin, kieselguhr or metal powder. In an example the novel epoxy-carbonate ester is hardened with phthalic anhydride and tris(dimethylaminomethyl)phenol.ALSO:The invention comprises compounds of the formula <FORM:0900506/IV (b)/1> which may be made by epoxidation of a compound of the formula <FORM:0900506/IV (b)/2> The epoxidation may be effected by treatment with organic peracids, e.g. peracetic, perbenzoic, peradipic or monoperphthalic acid, or by treatment in a first stage with hypochlorous acid and in a second stage with an HCl-eliminating agent, e.g. a strong alkali. Preferably peracetic acid is used at 0-40 DEG C. In addition to the di-epoxide, completely or partially hydrolysed epoxides arise from side reactions. The unsaturated ester starting material may be made by reaction of phosgene, in the presence of a tertiary base, with dehydronorborneol. The Provisional Specificagives general formulae in which the above compounds may be substituted on the ring carbon atoms by halogen, alkoxy or aliphatic, cycloaliphatic, araliphatic or aromatic hydrocarbon residues.
GB4377459A 1959-12-23 1959-12-23 Esters containing epoxide groups, their production and their uses Expired GB900506A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB4377459A GB900506A (en) 1959-12-23 1959-12-23 Esters containing epoxide groups, their production and their uses

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB4377459A GB900506A (en) 1959-12-23 1959-12-23 Esters containing epoxide groups, their production and their uses

Publications (1)

Publication Number Publication Date
GB900506A true GB900506A (en) 1962-07-04

Family

ID=10430258

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4377459A Expired GB900506A (en) 1959-12-23 1959-12-23 Esters containing epoxide groups, their production and their uses

Country Status (1)

Country Link
GB (1) GB900506A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007161652A (en) * 2005-12-14 2007-06-28 Daicel Chem Ind Ltd Method for producing alicyclic epoxy compound and alicyclic epoxy compound
WO2021033129A1 (en) 2019-08-17 2021-02-25 Prefere Resins Holding Gmbh Multifunctional cyclic organic carbonates as curing agents for organic compounds having phenolic hydroxyl groups
EP3786172A1 (en) 2019-09-02 2021-03-03 Prefere Resins Holding GmbH Multifunctional cyclic organic carbonates as curing agents for organic compounds having hydroxyl groups

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007161652A (en) * 2005-12-14 2007-06-28 Daicel Chem Ind Ltd Method for producing alicyclic epoxy compound and alicyclic epoxy compound
WO2021033129A1 (en) 2019-08-17 2021-02-25 Prefere Resins Holding Gmbh Multifunctional cyclic organic carbonates as curing agents for organic compounds having phenolic hydroxyl groups
EP3786172A1 (en) 2019-09-02 2021-03-03 Prefere Resins Holding GmbH Multifunctional cyclic organic carbonates as curing agents for organic compounds having hydroxyl groups

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