EP3033320A1 - Glycidyléthers de dérivés de divinylbenzène et oligomères desdits glycidyléthers de dérivés de divinylbenzène en tant que résine époxy durcissable - Google Patents

Glycidyléthers de dérivés de divinylbenzène et oligomères desdits glycidyléthers de dérivés de divinylbenzène en tant que résine époxy durcissable

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Publication number
EP3033320A1
EP3033320A1 EP14747946.3A EP14747946A EP3033320A1 EP 3033320 A1 EP3033320 A1 EP 3033320A1 EP 14747946 A EP14747946 A EP 14747946A EP 3033320 A1 EP3033320 A1 EP 3033320A1
Authority
EP
European Patent Office
Prior art keywords
glycidyl ether
glycidyl
group
atom
formula
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.)
Withdrawn
Application number
EP14747946.3A
Other languages
German (de)
English (en)
Inventor
Ulrich Karl
Monika CHARRAK
Hans-Josef Thomas
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 SE
Original Assignee
BASF SE
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 BASF SE filed Critical BASF SE
Priority to EP14747946.3A priority Critical patent/EP3033320A1/fr
Publication of EP3033320A1 publication Critical patent/EP3033320A1/fr
Withdrawn legal-status Critical Current

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Classifications

    • 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
    • C08G59/245—Di-epoxy compounds carbocyclic aromatic
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
    • C07C29/136—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
    • C07C29/14—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of a —CHO group
    • C07C29/141—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of a —CHO group with hydrogen or hydrogen-containing gases
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/36—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions with formation of hydroxy groups, which may occur via intermediates being derivatives of hydroxy, e.g. O-metal
    • C07C29/38—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions with formation of hydroxy groups, which may occur via intermediates being derivatives of hydroxy, e.g. O-metal by reaction with aldehydes or ketones
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C33/00—Unsaturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C33/18—Monohydroxylic alcohols containing only six-membered aromatic rings as cyclic part
    • C07C33/20—Monohydroxylic alcohols containing only six-membered aromatic rings as cyclic part monocyclic
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C33/00—Unsaturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C33/26—Polyhydroxylic alcohols containing only six-membered aromatic rings as cyclic part
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/01—Preparation of ethers
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C43/00—Ethers; Compounds having groups, groups or groups
    • C07C43/02—Ethers
    • C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
    • C07C43/14—Unsaturated ethers
    • C07C43/164—Unsaturated ethers containing six-membered aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/49—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide
    • C07C45/50—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide by oxo-reactions
    • 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
    • C07D303/18—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by etherified 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
    • C08G59/40—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 curing agents used
    • C08G59/50—Amines
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J163/00—Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Epoxy Resins (AREA)

Abstract

L'invention concerne des glycidyléthers de dérivés de divinylbenzène. Les résines époxy durcies sont largement répandues en raison de leurs propriétés mécaniques et chimiques exceptionnelles. On utilise habituellement des résines époxy à base de diglycidyléthers de bisphénol A ou bisphénol F, qui posent toutefois des problèmes dans de nombreux domaines en raison de leur effet endocrinien. La présente invention concerne des glycidyléthers de diols et/ou polyols à base de divinylbenzène et des compositions de résine époxy durcissable à base de ces derniers en lieu et place de diglycidyléthers de bisphénol A ou bisphénol F ou de compositions de résine époxy à base de ces derniers.
EP14747946.3A 2013-08-14 2014-08-07 Glycidyléthers de dérivés de divinylbenzène et oligomères desdits glycidyléthers de dérivés de divinylbenzène en tant que résine époxy durcissable Withdrawn EP3033320A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP14747946.3A EP3033320A1 (fr) 2013-08-14 2014-08-07 Glycidyléthers de dérivés de divinylbenzène et oligomères desdits glycidyléthers de dérivés de divinylbenzène en tant que résine époxy durcissable

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP13180427 2013-08-14
PCT/EP2014/066952 WO2015022253A1 (fr) 2013-08-14 2014-08-07 Glycidyléthers de dérivés de divinylbenzène et oligomères desdits glycidyléthers de dérivés de divinylbenzène en tant que résine époxy durcissable
EP14747946.3A EP3033320A1 (fr) 2013-08-14 2014-08-07 Glycidyléthers de dérivés de divinylbenzène et oligomères desdits glycidyléthers de dérivés de divinylbenzène en tant que résine époxy durcissable

Publications (1)

Publication Number Publication Date
EP3033320A1 true EP3033320A1 (fr) 2016-06-22

Family

ID=48951416

Family Applications (1)

Application Number Title Priority Date Filing Date
EP14747946.3A Withdrawn EP3033320A1 (fr) 2013-08-14 2014-08-07 Glycidyléthers de dérivés de divinylbenzène et oligomères desdits glycidyléthers de dérivés de divinylbenzène en tant que résine époxy durcissable

Country Status (4)

Country Link
US (1) US20160194436A1 (fr)
EP (1) EP3033320A1 (fr)
TW (1) TW201509924A (fr)
WO (1) WO2015022253A1 (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3146009A4 (fr) * 2014-05-19 2017-12-06 Valspar Sourcing, Inc. Polyéthers contenant des groupes cycliques non bisphénoliques
EP3268405B1 (fr) 2015-03-11 2023-10-25 Basf Se Procédé de fabrication de polyuréthane compact ayant une stabilité en hydrolyse améliorée
US11390578B2 (en) * 2018-04-06 2022-07-19 Basf Se Method for synthesizing amines

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2622550C (fr) * 2005-10-18 2014-03-25 Valspar Sourcing, Inc. Compositions de revetement pour contenants et procedes d'enduction

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
See also references of WO2015022253A1 *
SERGIO?A. CALDARELLI ET AL: "Synthesis and Evaluation of Bis-Thiazolium Salts as Potential Antimalarial Drugs", CHEMMEDCHEM, vol. 5, no. 7, 5 July 2010 (2010-07-05), pages 1102 - 1109, XP055450162, ISSN: 1860-7179, DOI: 10.1002/cmdc.201000097 *
TETSUO TAKEMURA ET AL: "Separation and characterization of all configurational isomers by enzymatic discrimination of each chiral function", TETRAHEDRON LETTERS, 1 January 1992 (1992-01-01), pages 6335 - 6338, XP055450129, Retrieved from the Internet <URL:http://www.sciencedirect.com/science/article/pii/S004040390060967X/pdf?md5=58b4f89def60394136d22aa518cceb7e&pid=1-s2.0-S004040390060967X-main.pdf> DOI: 10.1016/S0040-4039(00)60967-X *
YAJUN GAO ET AL: "2,2'-( p -Phenylenedimethylene)bis(propane-1,3-diol)", ACTA CRYSTALLOGRAPHICA SECTION C. CRYSTAL STRUCTURE COMMUNICATIONS, vol. 65, no. 1, 15 January 2009 (2009-01-15), DK, pages o170 - o170, XP055450173, ISSN: 0108-2701, DOI: 10.1107/S1600536808041688 *

Also Published As

Publication number Publication date
US20160194436A1 (en) 2016-07-07
WO2015022253A1 (fr) 2015-02-19
TW201509924A (zh) 2015-03-16

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Inventor name: THOMAS, HANS-JOSEF

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