WO2002030859A3 - Tertiäre divinylether, verfahren zu deren herstellung und deren verwendung - Google Patents

Tertiäre divinylether, verfahren zu deren herstellung und deren verwendung Download PDF

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Publication number
WO2002030859A3
WO2002030859A3 PCT/EP2001/011054 EP0111054W WO0230859A3 WO 2002030859 A3 WO2002030859 A3 WO 2002030859A3 EP 0111054 W EP0111054 W EP 0111054W WO 0230859 A3 WO0230859 A3 WO 0230859A3
Authority
WO
WIPO (PCT)
Prior art keywords
alkyl
cycloalkyl
substituted
tertiary
divinyl ethers
Prior art date
Application number
PCT/EP2001/011054
Other languages
English (en)
French (fr)
Other versions
WO2002030859A2 (de
Inventor
Thomas Preiss
Sabine Weiguny
Original Assignee
Basf Ag
Thomas Preiss
Sabine Weiguny
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 Ag, Thomas Preiss, Sabine Weiguny filed Critical Basf Ag
Priority to AU2002221625A priority Critical patent/AU2002221625A1/en
Publication of WO2002030859A2 publication Critical patent/WO2002030859A2/de
Publication of WO2002030859A3 publication Critical patent/WO2002030859A3/de

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F16/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical
    • C08F16/12—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an ether radical
    • C08F16/32—Monomers containing two or more unsaturated aliphatic radicals
    • 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
    • C07C43/15—Unsaturated ethers containing only non-aromatic carbon-to-carbon double bonds
    • C07C43/16—Vinyl ethers
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C43/00—Ethers; Compounds having groups, groups or groups
    • C07C43/02—Ethers
    • C07C43/18—Ethers having an ether-oxygen atom bound to a carbon atom of a ring other than a six-membered aromatic ring
    • C07C43/188—Unsaturated ethers
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00—Systems containing only non-condensed rings
    • C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/14—The ring being saturated

Landscapes

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

Abstract

Tertiäre Divinylether der Formel (I), in der R?1, R2, R3, R4¿ unabhängig voneinander: C¿1?- bis C20-Alkyl, jeweils unsubstituiert oder durch Alkyl oder Cycloalkyl substituiert; Cycloalky mit 3 bis 6 Ring-C-Atomen, jeweils unsubstituiert oder durch Alkyl oder Cycloalkyl substituiert; Phenyl, unsubstituiert oder durch Alkyl oder Cycloalkyl substituiert; oder R?1 und R2¿ gemeinsam oder R?3 und R4¿ gemeinsam C¿2?- bis C11-Alkylen, jeweils unsubstituiert oder durch Alkyl oder Cycloalkyl substituiert; R?5, R6¿ unabhängig voneinander: Wasserstoff; C1- bis C¿20?-Alkyl, jeweils unsubstituiert oder durch Alkyl oder Cycloalkyl substituiert; Cycloalkyl mit 3 bis 6 Ring-C-Atomen, jeweils unsubstituiert oder durch Alkyl oder Cycloalkyl substituiert; Phenyl, unsubstituiert oder durch Alkyl oder Cycloalkyl substituiert; X: Alkylen mit 1 bis 12 CH2-Gruppen bedeuten, deren Herstellung und Verwendung.
PCT/EP2001/011054 2000-09-30 2001-09-25 Tertiäre divinylether, verfahren zu deren herstellung und deren verwendung WO2002030859A2 (de)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU2002221625A AU2002221625A1 (en) 2000-09-30 2001-09-25 Tertiary divinyl ethers, method for the production and use thereof

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10048696.7 2000-09-30
DE10048696A DE10048696A1 (de) 2000-09-30 2000-09-30 Tertiäre Divinylether, Verfahren zu deren Herstellung und deren Verwendung

Publications (2)

Publication Number Publication Date
WO2002030859A2 WO2002030859A2 (de) 2002-04-18
WO2002030859A3 true WO2002030859A3 (de) 2002-11-14

Family

ID=7658362

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2001/011054 WO2002030859A2 (de) 2000-09-30 2001-09-25 Tertiäre divinylether, verfahren zu deren herstellung und deren verwendung

Country Status (3)

Country Link
AU (1) AU2002221625A1 (de)
DE (1) DE10048696A1 (de)
WO (1) WO2002030859A2 (de)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8084185B2 (en) * 2009-01-08 2011-12-27 International Business Machines Corporation Substrate planarization with imprint materials and processes
WO2015190376A1 (ja) * 2014-06-13 2015-12-17 丸善石油化学株式会社 新規なジビニルエーテル化合物およびその製造法
EP3889126A4 (de) * 2018-11-27 2022-08-17 Maruzen Petrochemical Co., Ltd. Verfahren zur herstellung einer divinyletherverbindung mit alkylenskelett
EP3889125A4 (de) * 2018-11-27 2022-08-17 Maruzen Petrochemical Co., Ltd. Verfahren zur herstellung einer divinyletherverbindung mit alkylenskelett

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1959927A (en) * 1930-10-30 1934-05-22 Ig Farbenindustrie Ag Production of vinyl ethers
DE1194407B (de) * 1959-11-02 1965-06-10 Hercules Powder Co Ltd Verfahren zur Herstellung von Vinylaethern tertiaerer Alkohole
US5352713A (en) * 1992-04-01 1994-10-04 Allied-Signal Inc. Free radical co-polymerization of acrylates and vinyl ethers

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1959927A (en) * 1930-10-30 1934-05-22 Ig Farbenindustrie Ag Production of vinyl ethers
DE1194407B (de) * 1959-11-02 1965-06-10 Hercules Powder Co Ltd Verfahren zur Herstellung von Vinylaethern tertiaerer Alkohole
US5352713A (en) * 1992-04-01 1994-10-04 Allied-Signal Inc. Free radical co-polymerization of acrylates and vinyl ethers

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
E. D. HOLLY: "Vinylation rates of primary, secondary, and tertiary alcohols", JOURNAL OF ORGANIC CHEMISTRY, vol. 24, 1959, EASTON US, pages 1752 - 1755, XP002170553 *

Also Published As

Publication number Publication date
DE10048696A1 (de) 2002-04-11
WO2002030859A2 (de) 2002-04-18
AU2002221625A1 (en) 2002-04-22

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