JP2007516976A5 - - Google Patents

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Publication number
JP2007516976A5
JP2007516976A5 JP2006544436A JP2006544436A JP2007516976A5 JP 2007516976 A5 JP2007516976 A5 JP 2007516976A5 JP 2006544436 A JP2006544436 A JP 2006544436A JP 2006544436 A JP2006544436 A JP 2006544436A JP 2007516976 A5 JP2007516976 A5 JP 2007516976A5
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JP
Japan
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group
carbon atoms
monovalent
substituted
general formula
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JP2006544436A
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English (en)
Japanese (ja)
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JP2007516976A (ja
JP4474419B2 (ja
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Priority claimed from PCT/EP2004/053492 external-priority patent/WO2005058788A1/en
Publication of JP2007516976A publication Critical patent/JP2007516976A/ja
Publication of JP2007516976A5 publication Critical patent/JP2007516976A5/ja
Application granted granted Critical
Publication of JP4474419B2 publication Critical patent/JP4474419B2/ja
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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JP2006544436A 2003-12-16 2004-12-15 グリコールアルデヒドの調製方法 Expired - Lifetime JP4474419B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP03257883 2003-12-16
PCT/EP2004/053492 WO2005058788A1 (en) 2003-12-16 2004-12-15 Process of preparing glycolaldehyde

Publications (3)

Publication Number Publication Date
JP2007516976A JP2007516976A (ja) 2007-06-28
JP2007516976A5 true JP2007516976A5 (https=) 2009-04-09
JP4474419B2 JP4474419B2 (ja) 2010-06-02

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ID=34684623

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2006544436A Expired - Lifetime JP4474419B2 (ja) 2003-12-16 2004-12-15 グリコールアルデヒドの調製方法

Country Status (11)

Country Link
US (2) US7449607B2 (https=)
EP (1) EP1697291A1 (https=)
JP (1) JP4474419B2 (https=)
KR (1) KR20060117345A (https=)
CN (1) CN100434412C (https=)
AU (1) AU2004298446B2 (https=)
BR (1) BRPI0417643A (https=)
CA (1) CA2549456A1 (https=)
MX (1) MXPA06006705A (https=)
RU (1) RU2371429C2 (https=)
WO (1) WO2005058788A1 (https=)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7858787B2 (en) * 2006-09-22 2010-12-28 Shell Oil Company Process for producing olefins
US7301054B1 (en) 2006-09-29 2007-11-27 Eastman Chemical Company Process for the preparation of glycolaldehyde
US7420093B2 (en) 2006-09-29 2008-09-02 Eastman Chemical Company Process for the preparation of glycolaldehyde
US7674937B2 (en) 2008-05-28 2010-03-09 Eastman Chemical Company Hydroformylation catalysts
FR2943061B1 (fr) * 2009-03-13 2011-02-25 Rhodia Operations Composes organophosphores, systemes catalytiques comprenant ces composes et procede d'hydrocyanation ou d'hydroformylation utilisant ces systemes catalytiques
JP5791628B2 (ja) 2009-12-17 2015-10-07 ビーエーエスエフ ソシエタス・ヨーロピアBasf Se 高級エタノールアミンの製造方法
EP2513036B1 (de) 2009-12-17 2019-04-17 Basf Se Umsetzung von glykolaldehyd mit einem aminierungsmittel
CN101811933B (zh) * 2010-04-26 2013-05-08 常州大学 一种催化合成乙二醇的方法
TWI508937B (zh) * 2014-04-30 2015-11-21 Chien An Chen 使用甲醇為原料經由甲醛、乙醇醛的中間產物而合成乙二醇的製造方法
CN105085211B (zh) * 2014-05-16 2017-09-05 陈建安 一种甲醛、乙醇醛及乙二醇的制造方法
MY184090A (en) * 2014-05-19 2021-03-17 Iowa Corn Promotion Board Process for the continuous production of ethylene glycol from carbohydrates
CN106470965B (zh) * 2014-06-30 2019-07-26 托普索公司 从糖制备乙二醇的方法
UA123868C2 (uk) 2016-01-07 2021-06-16 Хальдор Топсьое А/С Спосіб одержання етиленгліколю з цукрів
MX2018007750A (es) 2016-01-07 2018-11-14 Topsoe Haldor As Proceso para la preparacion de etilenglicol a partir de azucares.
CN105618035B (zh) * 2016-02-02 2018-05-11 中国科学院福建物质结构研究所 合成气制备乙醇醛所用的负载型铑催化剂及其制备方法
RU2759538C2 (ru) 2016-12-08 2021-11-15 Хальдор Топсёэ А/С Получение гликолевого альдегида термолитической фрагментацией
GB201904612D0 (en) 2019-04-02 2019-05-15 Univ Leuven Kath Reaction of glycoladehyde
WO2020095147A1 (en) * 2018-11-07 2020-05-14 Sabic Global Technologies B.V. Catalyst systems and methods for their use in selective hydroformylation of formaldehyde to glycolaldehyde
WO2020249428A1 (en) 2019-06-11 2020-12-17 Basf Se Products obtained by the conversion of glycolaldehyde derivatives and aminating agents and their conversion to ethyleneamines and ethanolamines
WO2020249426A1 (en) 2019-06-11 2020-12-17 Basf Se Conversion of glycolaldehyde with an aminating agent
CN114008016B (zh) 2019-06-11 2025-03-04 巴斯夫欧洲公司 通过乙醇醛衍生物和胺化剂的转化以及它们向亚乙基胺类和乙醇胺类的转化获得的产物
CN112337508A (zh) * 2020-11-03 2021-02-09 中国科学院福建物质结构研究所 一种乙醇醛合成用铑基催化剂及其制备方法
DE202021103519U1 (de) 2021-07-01 2021-07-16 Schill + Seilacher Gmbh Gerbmittel, Verwendung des Gerbmittels zum Gerben von Tierhäuten und Fellen und daraus erhaltenes Leder
ES2975566T3 (es) 2021-07-01 2024-07-09 Schill Seilacher Gmbh Agente curtiente, uso de un curtiente y procedimiento de curtido de pieles de animales y del cuero obtenido a partir de las mismas
CN114751813B (zh) * 2022-05-05 2023-12-15 天津大学 一种甲醛氢甲酰化制备乙醇醛的方法
CN115340440B (zh) * 2022-08-18 2024-09-06 山东能源集团有限公司 一种制备乙二醇的方法
CN115108887A (zh) * 2022-08-18 2022-09-27 山东能源集团有限公司 一种乙二醇的制备方法

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3026327A (en) 1960-07-06 1962-03-20 American Cyanamid Co Substituted 1, 3, 5, 7-tetraalkyl-2, 6, 9-trioxa-10-phosphatricyclo [3.3.1.1.3,7] decanes
US4414421A (en) * 1981-08-03 1983-11-08 Shell Oil Company Process for the preparation of glycol aldehyde
US4608444A (en) * 1984-04-05 1986-08-26 The Halcon Sd Group, Inc. Process and accompanying catalysts for the hydroformylation of formaldehyde to glycol-aldehyde
US4847423A (en) * 1988-03-03 1989-07-11 Hoechst Celanese Corporation Hydroformylation of aqueous formaldehyde using a rhodium-tricyclohexylphosphine catalyst system
SU1608182A1 (ru) * 1988-09-15 1990-11-23 Предприятие П/Я В-2287 Способ получени гликолевого альдегида
US5567856A (en) * 1995-05-30 1996-10-22 Hoechst Celanese Corporation Synthesis of and hydroformylation with fluoro-substituted bidentate phosphine ligands
US6156934A (en) * 1997-03-26 2000-12-05 Shell Oil Company Diphosphines
DE10023468A1 (de) 2000-05-12 2001-11-15 Basf Ag Verfahren zur Hydroformylierung ethylenisch ungesättigter Verbindungen und Ligand-Metall-Komplex als Katalysator hierfür

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