GB928449A - An ether containing epoxide groups, its production and its uses - Google Patents

An ether containing epoxide groups, its production and its uses

Info

Publication number
GB928449A
GB928449A GB1371460A GB1371460A GB928449A GB 928449 A GB928449 A GB 928449A GB 1371460 A GB1371460 A GB 1371460A GB 1371460 A GB1371460 A GB 1371460A GB 928449 A GB928449 A GB 928449A
Authority
GB
United Kingdom
Prior art keywords
compounds
epoxide groups
formula
ether product
epoxide
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
GB1371460A
Inventor
Keith Wood Humphreys
Bernard Peter Stark
Reginald Francis Webb
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 GB1371460A priority Critical patent/GB928449A/en
Priority to BE602740A priority patent/BE602740A/en
Publication of GB928449A publication Critical patent/GB928449A/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
    • C07D303/18Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by etherified hydroxyl radicals
    • C07D303/28Ethers with hydroxy compounds containing oxirane rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Epoxy Resins (AREA)

Abstract

A hardenable composition comprises an ether product containing two epoxide groups and being one or more of the isomeric compounds of the formula: <FORM:0928449/IV(a)/1> together with one or more hardening agents therefor, preferably polybasic carboxylic acids and their anhydrides. Other suitable hardeners are amines or amides, guanidine and guanidine derivatives, dicyandiamide, aniline-formaldehyde resins, polymers of amino-styrenes, polyamides, isocyanates, isothiocyanates, polyhydric phenols, phenol-aldehyde resins, reaction products of aluminium alkoxides or phenoxides with tauto meric reacting compounds of the aceto-acetic ester type, Friedel-Crafts catalysts and phosphoric acid. Accelerators may be present such as tertiary amines, polyhydroxy compounds, alkali metal alkoxides or carboxylic acids. The mixtures may also contain a proportion of the above ether product in which the epoxide groups are completely or partially hydrolysed to hydroxyl groups, or other polyhydroxy compounds. Other epoxides such as mono- or polyglycidyl ethers of mono- or poly-alcohols, polyglycidyl esters of polycarboxylic acids, or aminopolyepoxides, may also be present. The hardenable compositions also contain fillers, plasticizers or colouring agents. In an example, the bis-epoxide of bis-dihydrodicyclopentadienyl ether is heated to 120 DEG C. and cured with phthalic anhydride and benzyldimethylamine.ALSO:An ether product containing two epoxide groups and being one or more of the isomeric compounds of the formula: <FORM:0928449/IV(a)/1> is made by epoxidising one or more isomeric compounds of the formula: <FORM:0928449/IV(a)/2> for example by treatment with an organic peracid such as peracetic, perbenzoic, peradipic or monoperphthalic acid, preferably by treatment with peracetic acid at 0 DEG to 40 DEG C. A detailed example is given.
GB1371460A 1960-04-19 1960-04-19 An ether containing epoxide groups, its production and its uses Expired GB928449A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
GB1371460A GB928449A (en) 1960-04-19 1960-04-19 An ether containing epoxide groups, its production and its uses
BE602740A BE602740A (en) 1960-04-19 1961-04-18 Ether containing epoxy groups, its manufacture and uses

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1371460A GB928449A (en) 1960-04-19 1960-04-19 An ether containing epoxide groups, its production and its uses

Publications (1)

Publication Number Publication Date
GB928449A true GB928449A (en) 1963-06-12

Family

ID=10028034

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1371460A Expired GB928449A (en) 1960-04-19 1960-04-19 An ether containing epoxide groups, its production and its uses

Country Status (2)

Country Link
BE (1) BE602740A (en)
GB (1) GB928449A (en)

Also Published As

Publication number Publication date
BE602740A (en) 1961-10-18

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