ES2069259T3 - Procedimiento para la obtencion de n,n,n',n'-tetraglicidil-3,3'-dialquil-4,4'-diaminodifenilmetanos. - Google Patents

Procedimiento para la obtencion de n,n,n',n'-tetraglicidil-3,3'-dialquil-4,4'-diaminodifenilmetanos.

Info

Publication number
ES2069259T3
ES2069259T3 ES91810303T ES91810303T ES2069259T3 ES 2069259 T3 ES2069259 T3 ES 2069259T3 ES 91810303 T ES91810303 T ES 91810303T ES 91810303 T ES91810303 T ES 91810303T ES 2069259 T3 ES2069259 T3 ES 2069259T3
Authority
ES
Spain
Prior art keywords
sub
tetraglicidil
diaminodifenilmetanos
dialquil
procedure
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 - Lifetime
Application number
ES91810303T
Other languages
English (en)
Inventor
Werner Schaffner
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.)
Novartis AG
Original Assignee
Ciba Geigy 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 Geigy AG filed Critical Ciba Geigy AG
Application granted granted Critical
Publication of ES2069259T3 publication Critical patent/ES2069259T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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
    • C07D303/36—Compounds containing oxirane rings with hydrocarbon radicals, substituted by nitrogen atoms
    • 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
    • C08G59/32—Epoxy compounds containing three or more epoxy groups
    • C08G59/3227—Compounds containing acyclic nitrogen atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Epoxy Compounds (AREA)
  • Epoxy Resins (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

METODO PARA LA ELABORACION DE COMPOSICIONES DE LA FORMULA I DONDE R SIGNIFICA GLICIDIL, Y R SUB 1 Y R SUB 3 INDEPENDIENTEMENTE ENTRE SI, SON C SUB 1-C SUB 6 ALQUILO Y R SUB 2 Y R SUB 4 INDEPENDIENTEMENTE ENTRE SI SON HIDROGENO O METILO, Y SE CARACTERIZA PORQUE (I) UN DIAMIN DE LA FORMULA II SE TRANSFORMA EN EPICLORIDRIN EN UNA RELACION DE MOL DE 1:12 A 1:40 A UNA TEMPERATURA DE 80 A 115 C, DONDE R SUB 1, R SUB 2, R SUB 3 Y R SUB 4 TIENEN EL MISMO SIGNIFICADO ARRIBA MENCIONADO. (II) AÑADE A UNA MEZCLA DE REACCION UN CATALIZADOR DE FASENTRANSFER, QUE SOMETE A LA EPICLORIDRIN A UNA DESTILACION DE CIRCULACION Y SE LLEVA A CABO AL MISMO TIEMPO QUE LA DEHIDROCLORIZACION AL AÑADIR UNA DISOLUCION DE (TIERRA) DE ALCALIHIDROXID, AL MISMO TIEMPO QUE SE PRODUCE LA SEPARACION DEL AGUA DESTILADA DE AZEOTROP
ES91810303T 1990-05-07 1991-04-23 Procedimiento para la obtencion de n,n,n',n'-tetraglicidil-3,3'-dialquil-4,4'-diaminodifenilmetanos. Expired - Lifetime ES2069259T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH153790 1990-05-07

Publications (1)

Publication Number Publication Date
ES2069259T3 true ES2069259T3 (es) 1995-05-01

Family

ID=4212742

Family Applications (1)

Application Number Title Priority Date Filing Date
ES91810303T Expired - Lifetime ES2069259T3 (es) 1990-05-07 1991-04-23 Procedimiento para la obtencion de n,n,n',n'-tetraglicidil-3,3'-dialquil-4,4'-diaminodifenilmetanos.

Country Status (6)

Country Link
US (1) US5149841A (es)
EP (1) EP0456602B1 (es)
JP (1) JP3035671B2 (es)
CA (1) CA2041833C (es)
DE (1) DE59104649D1 (es)
ES (1) ES2069259T3 (es)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5132036B2 (ja) * 2005-03-29 2013-01-30 日本化薬株式会社 液状エポキシ樹脂、エポキシ樹脂組成物及びその硬化物
JP5028818B2 (ja) * 2006-02-21 2012-09-19 三菱瓦斯化学株式会社 テトラグリシジルアミノ化合物の製造方法
JPWO2011118349A1 (ja) * 2010-03-23 2013-07-04 東レ・ファインケミカル株式会社 高純度エポキシ化合物およびその製造方法
CN111777741B (zh) * 2020-08-04 2023-03-21 上海华谊树脂有限公司 四缩水甘油胺类环氧树脂及其制备方法
CN113698574A (zh) * 2021-09-14 2021-11-26 安徽新远科技股份有限公司 一种四官能缩水甘油胺型环氧树脂的合成方法
CN114591490B (zh) * 2022-04-24 2022-12-09 四川大学 一种缩水甘油胺型环氧树脂的合成方法

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1790042A (en) * 1926-08-03 1931-01-27 Winthrop Chem Co Substituted 1, 3-di-amino-2-propanols
US3278561A (en) * 1962-06-15 1966-10-11 Monsanto Co Hydrophobic diglycidylamines
US3595882A (en) * 1968-10-24 1971-07-27 Dow Chemical Co Process for preparing halogenated amine polyepoxides
JPS53124226A (en) * 1977-04-07 1978-10-30 Mitsubishi Gas Chem Co Inc Preparation of polyglycidyl compounds
DE2947469A1 (de) * 1979-11-24 1981-06-04 Hoechst Ag, 6000 Frankfurt Verfahren zur herstellung von glycidylaethern ein- oder mehrwertiger phenole
JPS5770881A (en) * 1980-10-20 1982-05-01 Mitsubishi Petrochem Co Ltd Preparation of polyepoxy compound
GB2111977A (en) * 1981-10-01 1983-07-13 Secr Defence Epoxy compounds containing N-diglycidyl groups
JPS59175481A (ja) * 1983-03-25 1984-10-04 Kanegafuchi Chem Ind Co Ltd 新規エポキシ樹脂およびその製造方法
DE3467577D1 (en) * 1983-09-29 1987-12-23 Ciba Geigy Ag Process for the preparation of n-glycidyl compounds
JPH0832697B2 (ja) * 1987-04-03 1996-03-29 三菱瓦斯化学株式会社 ポリグリシジルアミノ化合物の製造方法
US4778863A (en) * 1987-08-13 1988-10-18 The Dow Chemical Company Preparation of epoxy resins having low undesirable halogen content
JPH0277376A (ja) * 1988-09-12 1990-03-16 Sanyo Electric Co Ltd 自転車用表示装置

Also Published As

Publication number Publication date
JPH04225970A (ja) 1992-08-14
DE59104649D1 (de) 1995-03-30
JP3035671B2 (ja) 2000-04-24
CA2041833C (en) 2001-11-20
CA2041833A1 (en) 1991-11-08
EP0456602B1 (de) 1995-02-22
US5149841A (en) 1992-09-22
EP0456602A1 (de) 1991-11-13

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