GB900506A - Esters containing epoxide groups, their production and their uses - Google Patents
Esters containing epoxide groups, their production and their usesInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/12—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
- C07D303/16—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by esterified hydroxyl radicals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates 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
- C08G59/18—Macromolecules 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
- C08G59/20—Macromolecules 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
- C08G59/22—Di-epoxy compounds
- C08G59/24—Di-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.
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)
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 |
-
1959
- 1959-12-23 GB GB4377459A patent/GB900506A/en not_active Expired
Cited By (3)
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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