WO2007083519A1 - Méthode de production de polyéther-polyol - Google Patents

Méthode de production de polyéther-polyol Download PDF

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Publication number
WO2007083519A1
WO2007083519A1 PCT/JP2007/000013 JP2007000013W WO2007083519A1 WO 2007083519 A1 WO2007083519 A1 WO 2007083519A1 JP 2007000013 W JP2007000013 W JP 2007000013W WO 2007083519 A1 WO2007083519 A1 WO 2007083519A1
Authority
WO
WIPO (PCT)
Prior art keywords
group
polyether polyol
reaction
producing
polyol
Prior art date
Application number
PCT/JP2007/000013
Other languages
English (en)
Japanese (ja)
Inventor
Takanori Taniguchi
Masaki Takai
Original Assignee
Mitsubishi Chemical Corporation
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 Mitsubishi Chemical Corporation filed Critical Mitsubishi Chemical Corporation
Publication of WO2007083519A1 publication Critical patent/WO2007083519A1/fr

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Classifications

    • 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
    • C08G65/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/34Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives

Definitions

  • the heterocyclic aromatic ammonium salt and the aliphatic ammonium salt represented by the above general formula (1) are preferable, and the reaction rate is large and the product is less colored.
  • the aliphatic ammonium salt represented by 1) is more preferred.
  • R ' includes an alkyl group containing a substituent and an aryl group. More specifically, examples thereof include a linear hydrocarbon group, a branched hydrocarbon group, an alicyclic hydrocarbon group, an aralkyl group, a fluoroalkyl group, a vinyl group, and a naphthyl group.
  • Examples of the alicyclic hydrocarbon group include a cyclopropyl group, a cyclopentyl group, a cyclohexyl group, a methylcyclohexyl group, and a cycloheptyl group.
  • Examples of the aralkyl group include a benzyl group, a 2_phenylethyl group, and a 3-phenylpropyl group.
  • the compound include trimethylsulfonium bumbamide, tri_n_ butylsulfonyl bumudide, triphenyl sulfonyl bubutamide, tri-P-tolyl sulfonyl trifluoromethanesulfonate, dimethyl (methyl) (Luthio) sulfone tetrafluoroborate, (2-carboxyethyl) dimethyl sulfone chloride, diphenyl (methyl) sulfone tetrafluoroporate, and the like.
  • the poly (ethylene methylene ether) glycol obtained by the method of the present invention can be used for applications such as elastic fibers, thermoplastic polyester elastomers, thermoplastic polyurethane elastomers, and coating materials.
  • the degree of coloring of the polyether polyol is determined by the Hazen color number.
  • Example 1 The same operation as in Example 1 was conducted except that 0.008 g (0.329 mmo I) of tetramethylammonium sulfate was used instead of N-methylpyridinium chloride in Example 1. Thus, poly (polymethylene ether glycol) was obtained. The results are shown in Table 1.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyethers (AREA)

Abstract

La présente invention concerne une méthode de production d'un polyéther-polyol, très peu coloré malgré un degré de polymérisation élevé, avec un rendement élevé par le biais de la déshydratation-condensation d'un polyol. Lorsqu'un polyéther-polyol est produit par réaction de déshydratation-condensation d'un polyol, cette réaction est menée en présence d'un sel d'onium. Au moins un sel sélectionné parmi les sels d'ammonium et les sels de phosphonium est de préférence utilisé au titre de sel d'onium.
PCT/JP2007/000013 2006-01-20 2007-01-16 Méthode de production de polyéther-polyol WO2007083519A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2006-012458 2006-01-20
JP2006012458 2006-01-20

Publications (1)

Publication Number Publication Date
WO2007083519A1 true WO2007083519A1 (fr) 2007-07-26

Family

ID=38287473

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2007/000013 WO2007083519A1 (fr) 2006-01-20 2007-01-16 Méthode de production de polyéther-polyol

Country Status (1)

Country Link
WO (1) WO2007083519A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113603659A (zh) * 2021-07-16 2021-11-05 江苏海田技术有限公司 一种丙烯酸羟乙基邻苯二甲酸缩水甘油酯及其制备方法

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06503113A (ja) * 1990-11-27 1994-04-07 コモンウェルス・サイエンティフィック・アンド・インダストリアル・リサーチ・オーガナイゼーション ポリ(アルキレンオキシド)類
JP2003138009A (ja) * 2001-10-31 2003-05-14 Sumitomo Chem Co Ltd 芳香族ポリエーテルの製造方法
JP2003517071A (ja) * 1999-12-17 2003-05-20 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー ポリトリメチレンエーテルグリコールおよびそのコポリマーの生成
WO2004048440A1 (fr) * 2002-11-22 2004-06-10 Mitsubishi Chemical Corporation Procede permettant de produire du polyol de polyether
WO2004099110A1 (fr) * 2003-05-08 2004-11-18 Mitsubishi Chemical Corporation Procede de production de 1,3-propane diol
WO2006001482A1 (fr) * 2004-06-29 2006-01-05 Mitsubishi Chemical Corporation Procédé servant à produre un polyéther de polyol

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06503113A (ja) * 1990-11-27 1994-04-07 コモンウェルス・サイエンティフィック・アンド・インダストリアル・リサーチ・オーガナイゼーション ポリ(アルキレンオキシド)類
JP2003517071A (ja) * 1999-12-17 2003-05-20 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー ポリトリメチレンエーテルグリコールおよびそのコポリマーの生成
JP2003138009A (ja) * 2001-10-31 2003-05-14 Sumitomo Chem Co Ltd 芳香族ポリエーテルの製造方法
WO2004048440A1 (fr) * 2002-11-22 2004-06-10 Mitsubishi Chemical Corporation Procede permettant de produire du polyol de polyether
WO2004099110A1 (fr) * 2003-05-08 2004-11-18 Mitsubishi Chemical Corporation Procede de production de 1,3-propane diol
WO2006001482A1 (fr) * 2004-06-29 2006-01-05 Mitsubishi Chemical Corporation Procédé servant à produre un polyéther de polyol

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113603659A (zh) * 2021-07-16 2021-11-05 江苏海田技术有限公司 一种丙烯酸羟乙基邻苯二甲酸缩水甘油酯及其制备方法

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