GB951399A - New acetals containing epoxy groups - Google Patents

New acetals containing epoxy groups

Info

Publication number
GB951399A
GB951399A GB3171760A GB3171760A GB951399A GB 951399 A GB951399 A GB 951399A GB 3171760 A GB3171760 A GB 3171760A GB 3171760 A GB3171760 A GB 3171760A GB 951399 A GB951399 A GB 951399A
Authority
GB
United Kingdom
Prior art keywords
formula
radical
cycloaliphatic
araliphatic
aliphatic
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
GB3171760A
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
Original Assignee
Ciba AG
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 filed Critical Ciba AG
Publication of GB951399A publication Critical patent/GB951399A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D407/00Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/14Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D317/00Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/10Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
    • C07D317/14Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D317/18Radicals substituted by singly bound oxygen or sulfur atoms
    • C07D317/20Free hydroxyl or mercaptan
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D319/00Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D319/041,3-Dioxanes; Hydrogenated 1,3-dioxanes
    • C07D319/061,3-Dioxanes; Hydrogenated 1,3-dioxanes not condensed with other rings
    • 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
    • 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
    • C08G59/26Di-epoxy compounds heterocyclic

Landscapes

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

Abstract

The invention comprises acetals containing at least two epoxide groups and of the formula: <FORM:0951399/C2/1> in which R1 to R9 each represent a hydrogen atom or a monovalent substituent such as a halogen atom, an alkoxy group or an aliphatic, cycloaliphatic, araliphatic or aromatic hydrocarbon residue, and R1 and R5 together may also represent an alkylene radical such as a methylene group; #Z represents a trivalent aliphatic, cycloaliphatic or araliphatic hydrocarbon residue with at least 3 carbon atoms, none of which has more than a single free valence, and no carbon having such a free valence carries a hydroxyl group; n is 1 or 2; and, when n is 1, G is a radical of formula -#O-#U1 or -#O-C#O-#U1, where #U1 is an organic radical containing an epoxide group and, when n is 2, G is a radical of the formula -#O-, -#O-C#O-#O-, -#O-C#O-C#O-#O, or -#OC#O-#U2-#O-C#O-, where #U2 is an aliphatic, cycloaliphatic, araliphatic, or aromatic hydrocarbon radical. The epoxy compounds may be obtained by epoxidation of the compounds having a formula: <FORM:0951399/C2/2> in which when n is 1, G1 is -#O#U1 1 or -#OC#O#U1 1 where #U1 1 is an organic radical containing an epoxidisable group, such as a double bond or halohydrin grouping. The double bonds may be epoxidised with a peracid such as peracetic, perbenzoic, peradipic or mono-perphthalic acid, or by reaction with H#OCI followed by treatment with strong alkali. The unsaturated starting materials (IV) may be made by acetalising a D 3-tetra-hydrobenzaldehyde with a polyalcohol (H#O)2#Z-#C, where #C may be #O#H, Cl or Br., in the presence of an acid catalyst, or with an epoxide #O = #Z-#C. The product is an acetal of formula: <FORM:0951399/C2/3> This acetal may be converted to (IV) by etherification, esterification or re-esterification with a compound containing one or more reactive halogen atoms or groups containing active hydrogen atoms. Suitable types of compounds are epihalohydrins, dihalohydrins, unsaturated alcohols, glycerol diesters of unsaturated fatty acids, unsaturated carboxylic acids and functional derivatives, unsaturated halides, unsaturated acetals, carbonic acid, phosgene, and polycarboxylic acids, their acid halides or anhydrides. The acetals (IV) may also be made by acetalising the D 3-tetrahydrobenzaldehyde with a polyol of the formula (#H#O)2 #Z-G-#Z(#O#H)2, e.g., diglycerol, or with a dialcohol (#H#O)2 #Z-G1 such as an adduct of glycerol with dicyclopentadiene, or glycerol-monoallyl ether with cyclo-pentadiene. The preferred compounds of the invention are those of the formula: <FORM:0951399/C2/4> where R and R1 each represents hydrogen or C1-4 alkyl; Y2 is an aliphatic, cycloaliphatic, araliphatic or aromatic hydrocarbon residue, and m and n are each 1 or 2, and those of the formula: <FORM:0951399/C2/5> in which R and R1 each represents hydrogen or C1-4 alkyl. Specification 932,960 is referred to.ALSO:Curable mixtures comprise at least one acetal of the formula: <FORM:0951399/C3/1> wherein R1 to R9 are hydrogen or monovalent substituents such as halogen, alkoxy or aliphatic cycloaliphatic, araliphatic or aromatic hydrocarbon residues, and R1 and R5 together may also represent an alkylene radical such as a methylene group; Z is a trivalent aliphatic, cycloaliphatic or araliphatic hydrocarbon residue with at least 3 carbon atoms, none of which has more than a single free valence, and no carbon having such a free valence carries a hydroxyl group; n is 1 or 2, and, when n is 1, G is a radical of formula -O-Y1- or -O-CO-Y1, where Y1 is an organic radical containing an epoxide group and, when n is 2, G is a radical of the formula -O-, -O-CO-O, -O-CO-CO-O-, or -OCO -Y2-OCO-, where Y2 is an aliphatic, cycloaliphatic, araliphatic or aromatic radical, together with a curing agent for epoxy resins. The curing agent is preferably an anhydride of a dicarboxylic, or polycarboxylic acid. Other suitable curing agents are amines and amides, dicyandiamides, formaldehyde resins with aniline, urea and melamine; polymers of aminostyrenes, polyamides, isocyanates, isothiocyanates, polyhydric phenols, phenol-aldehyde resins, reaction products of aluminium alcoholates and phenolates with compounds of tautomeric reaction, Friedel-Crafts catalysts, metal fluoborates and phosphoric acid. An accelerator such as a tertiary amine or a strong Lewis base and advantageously also a polyhydroxy compound, may be added. The curable mixtures may also contain a proportion of the above acetals whose epoxide groups have been wholly or partially hydrolysed to hydroxyl groups, and/or also other cross-linking polyhydroxy compounds, such as hexanetriol. Other epoxides, such as mono-glycidyl or polyglycidyl ethers of mono- or polyalcohols, or of mono- or polyphenols, polyglycidyl esters of polycarboxylic acids, or amino-polyepoxides. Fillers, plasticizers and colouring matters may be added. Specification 932,960 is referred to.
GB3171760A 1959-09-17 1960-09-14 New acetals containing epoxy groups Expired GB951399A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
CH1191864A CH393362A (en) 1959-09-17 1959-09-17 Process for the production of new acetals containing epoxy groups
CH7833459A CH393360A (en) 1959-09-17 1959-09-17 Process for the production of new acetals containing epoxy groups
CH337460 1960-03-25

Publications (1)

Publication Number Publication Date
GB951399A true GB951399A (en) 1964-03-04

Family

ID=27174289

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3171760A Expired GB951399A (en) 1959-09-17 1960-09-14 New acetals containing epoxy groups

Country Status (5)

Country Link
CH (2) CH393360A (en)
DE (1) DE1443230A1 (en)
FR (1) FR1269917A (en)
GB (1) GB951399A (en)
NL (4) NL127414C (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013227579A (en) * 2006-07-28 2013-11-07 Givaudan Sa Method of using organic compounds
CN113667097A (en) * 2021-03-26 2021-11-19 蓝赛夫(上海)电子材料有限公司 Intermediate compound of epoxy resin monomer and preparation method and application thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013227579A (en) * 2006-07-28 2013-11-07 Givaudan Sa Method of using organic compounds
CN113667097A (en) * 2021-03-26 2021-11-19 蓝赛夫(上海)电子材料有限公司 Intermediate compound of epoxy resin monomer and preparation method and application thereof
CN113667097B (en) * 2021-03-26 2024-01-23 蓝赛夫(上海)电子材料有限公司 Intermediate compound of epoxy resin monomer, preparation method and application thereof

Also Published As

Publication number Publication date
NL255957A (en)
NL130093C (en)
FR1269917A (en) 1961-08-18
NL302591A (en)
CH393362A (en) 1965-06-15
DE1443230A1 (en) 1968-10-31
NL127414C (en)
CH393360A (en) 1965-06-15

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