JP2014525898A5 - - Google Patents

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Publication number
JP2014525898A5
JP2014525898A5 JP2014515897A JP2014515897A JP2014525898A5 JP 2014525898 A5 JP2014525898 A5 JP 2014525898A5 JP 2014515897 A JP2014515897 A JP 2014515897A JP 2014515897 A JP2014515897 A JP 2014515897A JP 2014525898 A5 JP2014525898 A5 JP 2014525898A5
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JP
Japan
Prior art keywords
secondary amine
methide
phenyl
tert
quinone methide
Prior art date
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Application number
JP2014515897A
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English (en)
Japanese (ja)
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JP5918362B2 (ja
JP2014525898A (ja
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Priority claimed from US13/158,958 external-priority patent/US8884038B2/en
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Publication of JP2014525898A publication Critical patent/JP2014525898A/ja
Publication of JP2014525898A5 publication Critical patent/JP2014525898A5/ja
Application granted granted Critical
Publication of JP5918362B2 publication Critical patent/JP5918362B2/ja
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JP2014515897A 2011-06-13 2012-06-11 7―アセチレンキノンメチド誘導体の合成及びそのビニル重合遅延剤としての用途 Active JP5918362B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US13/158,958 US8884038B2 (en) 2011-06-13 2011-06-13 Synthesis of 7-acetyleno quinone methide derivatives and their application as vinylic polymerization retarders
US13/158,958 2011-06-13
PCT/US2012/041823 WO2012173909A2 (en) 2011-06-13 2012-06-11 Synthesis of 7-acetyleno quinone methide derivatives and their application as vinylic polymerization retarders

Publications (3)

Publication Number Publication Date
JP2014525898A JP2014525898A (ja) 2014-10-02
JP2014525898A5 true JP2014525898A5 (https=) 2015-05-14
JP5918362B2 JP5918362B2 (ja) 2016-05-18

Family

ID=47292360

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2014515897A Active JP5918362B2 (ja) 2011-06-13 2012-06-11 7―アセチレンキノンメチド誘導体の合成及びそのビニル重合遅延剤としての用途

Country Status (12)

Country Link
US (2) US8884038B2 (https=)
EP (1) EP2718254B1 (https=)
JP (1) JP5918362B2 (https=)
KR (1) KR101951903B1 (https=)
CN (1) CN103619797B (https=)
BR (2) BR112013031103B1 (https=)
CA (1) CA2835868C (https=)
ES (1) ES2633763T3 (https=)
MX (1) MX355215B (https=)
SG (1) SG194960A1 (https=)
TW (1) TWI596087B (https=)
WO (1) WO2012173909A2 (https=)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8901362B2 (en) * 2012-02-02 2014-12-02 General Electric Company Methods and compositions for styrene inhibition via in situ generation of quinone methides
DE102013204950A1 (de) 2013-03-20 2014-09-25 Evonik Industries Ag Verfahren und Zusammensetzung zur Inhibierung der Polymerisation von Cyclopentadienverbindungen
CN104341281A (zh) * 2014-06-29 2015-02-11 浙江大学 2,6-二叔丁基-4-(2-甲氧基苯亚甲基)-2,5-环己二烯-1-酮及其制备法
WO2016061120A1 (en) 2014-10-14 2016-04-21 Ecolab Usa Inc. Reducing polymer fouling and agglomeration in acrylate/methacrylate processes
JP6730303B2 (ja) 2015-03-18 2020-07-29 エコラブ ユーエスエイ インク ビニルモノマーの重合を阻害するための安定した親油性ヒドロキシルアミン化合物の使用
US9957209B2 (en) 2015-03-31 2018-05-01 Ecolab Usa Inc. Use of quinone methides as antipolymerants for vinylic monomers
KR102616836B1 (ko) 2015-04-20 2023-12-20 에코랍 유에스에이 인코퍼레이티드 불포화 단량체에 대한 방오제로서의 입체 장애 하이드로퀴논
US11180578B2 (en) 2018-07-13 2021-11-23 Ecolab Usa Inc. Polymerization inhibitor and retarder compositions with amine stabilizer
EP3820836A1 (en) 2018-07-13 2021-05-19 Ecolab USA, Inc. Compositions of oxygenated amines and quinone methides as antifoulants for vinylic monomers
CN116553996A (zh) * 2023-07-07 2023-08-08 吉林金海化工新材料有限公司 一种阻聚剂及其应用

Family Cites Families (23)

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US2459597A (en) 1945-05-16 1949-01-18 Gulf Research Development Co Di-alkylated mono-hydroxy phenol
US3257321A (en) 1960-09-01 1966-06-21 Ethyl Corp 3, 5-dialkyl-4-hydroxybenzyl chloride
US3390198A (en) 1965-12-16 1968-06-25 Koppers Co Inc Tertiary-butyl-5-methyl catechol as polymerization inhibitor for hot styrene
US3660505A (en) 1969-08-27 1972-05-02 Exxon Research Engineering Co Hindered alkenyl phenols from quinone methide
US4003800A (en) 1976-01-02 1977-01-18 Gulf Research & Development Company Styrene purification process
US4032547A (en) 1976-02-23 1977-06-28 Gulf Research & Development Company Quinone alkide synthesis system
US4409408A (en) 1982-09-24 1983-10-11 Atlantic Richfield Company Inhibiting polymerization of vinyl aromatic monomers
US5446220A (en) 1994-08-24 1995-08-29 Betz Laboratories, Inc. Methods for inhibiting vinyl aromatic monomer polymerization
US5583247A (en) * 1995-04-14 1996-12-10 Ciba-Geigy Corporation 7-substituted quinone methides as inhibitors for unsaturated monomers
US5616774A (en) 1995-04-14 1997-04-01 Ciba-Geigy Corporation Inhibition of unsaturated monomers with 7-aryl quinone methides
EP0744392A1 (en) * 1995-05-26 1996-11-27 Ciba-Geigy Ag A new one-pot process for the preparation of 7-aryl-2,6-disubstituted quinone methides
FR2746098B1 (fr) * 1996-03-14 1998-04-30 Composes propynyl biaromatiques
US6024894A (en) 1998-03-25 2000-02-15 Betzdearborn Inc. Compositions and methods for inhibiting vinyl aromatic monomer polymerization
ES2292487T3 (es) * 1999-12-03 2008-03-16 Chemtura Corporation Composicion y metodo para inhibir la polimerizacion y el crecimiento polimerico.
US7045647B2 (en) 2000-10-16 2006-05-16 Uniroyal Chemical Company, Inc. Blends of quinone alkide and nitroxyl compounds and polymerization inhibitors
ES2247332T3 (es) 2001-03-20 2006-03-01 Ciba Specialty Chemicals Holding Inc. Composiciones ignifugantes.
US6926820B2 (en) 2002-09-20 2005-08-09 G.E. Betz, Inc. Inhibition of viscosity increase and fouling in hydrocarbon streams including unsaturation
US6818027B2 (en) 2003-02-06 2004-11-16 Ecoem, L.L.C. Organically clean biomass fuel
WO2004083156A1 (ja) 2003-03-17 2004-09-30 Hakuto Co., Ltd. 芳香族ビニル化合物の重合抑制剤および重合抑制方法
US20080132726A1 (en) * 2006-11-30 2008-06-05 Vinod Kumar Rai Process for the production of quinone methide
DE102007052891A1 (de) * 2007-11-02 2009-05-07 Evonik Degussa Gmbh Verfahren zur Stabilisierung von olefinisch ungesättigten Monomeren
US8247593B2 (en) 2008-05-13 2012-08-21 Nalco Company Process for preparing substituted 7-cyano quinone methides
US7651635B1 (en) 2009-02-05 2010-01-26 Nalco Company Polymer inhibition of vinyl aromatic monomers using a quinone methide/alkyl hydroxylamine combination

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