CN1089742C - 制备1,6-己二醇和己内酯的方法 - Google Patents

制备1,6-己二醇和己内酯的方法 Download PDF

Info

Publication number
CN1089742C
CN1089742C CN97192521A CN97192521A CN1089742C CN 1089742 C CN1089742 C CN 1089742C CN 97192521 A CN97192521 A CN 97192521A CN 97192521 A CN97192521 A CN 97192521A CN 1089742 C CN1089742 C CN 1089742C
Authority
CN
China
Prior art keywords
ester
esterification
cut
cyclohexanediol
caprolactone
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
CN97192521A
Other languages
English (en)
Chinese (zh)
Other versions
CN1211969A (zh
Inventor
K·G·保尔
R·费舍尔
R·宾克斯
F·斯坦恩
B·布里特施德尔
H·鲁斯特
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.)
BASF SE
Original Assignee
BASF SE
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
Priority claimed from DE1996107954 external-priority patent/DE19607954A1/de
Priority claimed from DE1996147349 external-priority patent/DE19647349A1/de
Application filed by BASF SE filed Critical BASF SE
Publication of CN1211969A publication Critical patent/CN1211969A/zh
Application granted granted Critical
Publication of CN1089742C publication Critical patent/CN1089742C/zh
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D315/00Heterocyclic compounds containing rings having one oxygen atom as the only ring hetero atom according to more than one of groups C07D303/00 - C07D313/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/132Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
    • C07C29/136Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
    • C07C29/147Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of carboxylic acids or derivatives thereof
    • C07C29/149Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of carboxylic acids or derivatives thereof with hydrogen or hydrogen-containing gases
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/74Separation; Purification; Use of additives, e.g. for stabilisation
    • C07C29/76Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment
    • C07C29/80Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment by distillation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/74Separation; Purification; Use of additives, e.g. for stabilisation
    • C07C29/88Separation; Purification; Use of additives, e.g. for stabilisation by treatment giving rise to a chemical modification of at least one compound
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C31/00Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C31/18Polyhydroxylic acyclic alcohols
    • C07C31/20Dihydroxylic alcohols
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/16Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
    • C07C51/31Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation of cyclic compounds with ring-splitting
    • C07C51/313Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation of cyclic compounds with ring-splitting with molecular oxygen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D313/00Heterocyclic compounds containing rings of more than six members having one oxygen atom as the only ring hetero atom
    • C07D313/02Seven-membered rings
    • C07D313/04Seven-membered rings not condensed with other rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/12Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/14The ring being saturated

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Polyesters Or Polycarbonates (AREA)
  • Pyrane Compounds (AREA)
CN97192521A 1996-03-01 1997-02-28 制备1,6-己二醇和己内酯的方法 Expired - Lifetime CN1089742C (zh)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
DE19607954.3 1996-03-01
DE1996107954 DE19607954A1 (de) 1996-03-01 1996-03-01 Verfahren zur Herstellung von 1,6-Hexandiol und Caprolacton
DE1996147349 DE19647349A1 (de) 1996-11-15 1996-11-15 Verfahren zur Herstellung von 1,6-Hexandiol und Caprolacton
DE19647349.7 1996-11-15

Publications (2)

Publication Number Publication Date
CN1211969A CN1211969A (zh) 1999-03-24
CN1089742C true CN1089742C (zh) 2002-08-28

Family

ID=26023397

Family Applications (1)

Application Number Title Priority Date Filing Date
CN97192521A Expired - Lifetime CN1089742C (zh) 1996-03-01 1997-02-28 制备1,6-己二醇和己内酯的方法

Country Status (13)

Country Link
US (1) US5981769A (cg-RX-API-DMAC7.html)
EP (1) EP0883591B1 (cg-RX-API-DMAC7.html)
JP (1) JP4107396B2 (cg-RX-API-DMAC7.html)
KR (1) KR100468182B1 (cg-RX-API-DMAC7.html)
CN (1) CN1089742C (cg-RX-API-DMAC7.html)
AT (1) ATE192730T1 (cg-RX-API-DMAC7.html)
CA (1) CA2248004C (cg-RX-API-DMAC7.html)
DE (1) DE59701646D1 (cg-RX-API-DMAC7.html)
ES (1) ES2147435T3 (cg-RX-API-DMAC7.html)
GR (1) GR3033955T3 (cg-RX-API-DMAC7.html)
MY (1) MY118128A (cg-RX-API-DMAC7.html)
PT (1) PT883591E (cg-RX-API-DMAC7.html)
WO (1) WO1997031883A1 (cg-RX-API-DMAC7.html)

Families Citing this family (43)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19757554A1 (de) 1997-12-23 1999-06-24 Basf Ag Verfahren zur Herstellung von 1,6-Hexandiol
DE19826614A1 (de) * 1998-05-29 1999-12-02 Basf Ag Verfahren zur Herstellung von Hexandiol-1,6
US6344586B1 (en) * 1998-07-30 2002-02-05 Sumitomo Chemical Company, Limited Process for producing adipic acid
ES2254402T3 (es) * 2000-08-24 2006-06-16 UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION Procedimientos para la fabricacion de lactonas.
DE10100552A1 (de) * 2001-01-09 2002-07-11 Basf Ag Verfahren und Vorrichtung zur destillativen Aufarbeitung von 1,6-Hexandiol, 1,5-Pentandiol ung Caprolacton
DE10128249A1 (de) * 2001-06-11 2002-12-12 Basf Ag Verfahren zur Entfernung von Ameisensäure aus wässrigen Lösungen
DE10242882A1 (de) * 2002-09-16 2004-03-25 Basf Ag Verfahren zur Herstellung von 1,6-Hexandiol
AU2003285106A1 (en) * 2002-11-01 2004-06-07 Cargill, Incorporated Process for preparation of 1,3-propanediol
WO2005121380A1 (en) * 2004-06-04 2005-12-22 Smithkline Beecham Corporation Predictive biomarkers in cancer therapy
DE102004033557A1 (de) 2004-07-09 2006-02-16 Basf Ag Verfahren zur Herstellung von 1,6-Hexandiol in einer Reinheit von über 99,5%
DE102004054047A1 (de) 2004-11-05 2006-05-11 Basf Ag Verfahren zur Herstellung von 1,6-Hexandiol
ATE458771T1 (de) * 2005-06-03 2010-03-15 Univ Twente Verzweigte polymere, ein makromonomer, verfahren zu deren herstellungen und deren verwendungen
EP1975146B1 (en) * 2006-01-13 2018-03-14 Ube Industries, Ltd. Process for production of 1,6-hexanediol
CA2690867A1 (en) * 2007-06-14 2008-12-18 Basf Se Process for preparing .epsilon.-caprolactone
EP2217587B1 (de) * 2007-11-05 2015-09-23 Basf Se Verfahren zur herstellung von e-caprolacton
US8217186B2 (en) 2007-12-21 2012-07-10 Basf Se Process for preparing epsilon-caprolactone
ES2393838T5 (es) 2008-02-15 2016-03-02 Basf Se Procedimiento para la obtención de ésteres de ácido 6-hidroxicaprónico
KR100922998B1 (ko) * 2008-03-06 2009-10-22 한국화학연구원 모노카르복실산 또는 그의 유도체로부터 일가 알콜의 제조방법
US8828903B2 (en) 2008-11-10 2014-09-09 Basf Corporation Copper catalyst for dehydrogenation application
US20110263907A1 (en) * 2008-12-05 2011-10-27 Basf Se Process for preparing 1,6-hexanediol
JP5651126B2 (ja) * 2008-12-18 2015-01-07 インヴィスタ テクノロジーズ エスアエルエル シクロヘキサン酸化工程副生成物の誘導体およびそれの使用方法
EP2385933B1 (de) 2009-01-12 2014-06-25 Basf Se Verfahren zur herstellung von polymethylolen
CA2755696A1 (en) * 2009-04-07 2010-10-14 Basf Se Method for producing 1,6-hexanediol
US8471042B2 (en) * 2009-04-07 2013-06-25 Basf Se Method for producing 1,6-hexanediol and caprolactone
TWI490034B (zh) 2009-11-17 2015-07-01 Basf Se 製備具有增強氫化活性之經承載氫化觸媒之方法
CA2800282A1 (en) * 2010-06-16 2011-12-22 Bioamber S.A.S. Processes for the production of hydrogenated products and derivatives thereof
KR20130041905A (ko) 2010-06-16 2013-04-25 바이오엠버, 에스.아.에스. 수소화 생성물 및 이의 유도체를 제조하는 방법
EP2404889A1 (de) * 2010-07-06 2012-01-11 LANXESS Deutschland GmbH Verfahren zur Herstellung von Alpha, Omega-Diolen
US20120059174A1 (en) * 2010-09-08 2012-03-08 Basf Se Process for preparing epsilon-caprolactone and 1,6-hexanediol
CN103080098B (zh) * 2010-09-08 2014-11-05 巴斯夫欧洲公司 制备ε-己内酯和1,6-己二醇的方法
WO2013101969A1 (en) 2011-12-30 2013-07-04 E. I. Du Pont De Nemours And Company Process for preparing 1, 6-hexanediol
US8865940B2 (en) 2011-12-30 2014-10-21 E I Du Pont De Nemours And Company Process for preparing 1,6-hexanediol
US8889912B2 (en) 2011-12-30 2014-11-18 E I Du Pont De Nemours And Company Process for preparing 1,6-hexanediol
US8884036B2 (en) 2011-12-30 2014-11-11 E I Du Pont De Nemours And Company Production of hydroxymethylfurfural from levoglucosenone
WO2013101977A1 (en) 2011-12-30 2013-07-04 E. I. Du Pont De Nemours And Company Production of tetrahydrofuran-2, 5-dimethanol from isosorbide
EP2797868A4 (en) 2011-12-30 2015-08-12 Du Pont PROCESS FOR PRODUCING HEXANEDIOLS
CN102603446B (zh) * 2012-02-13 2014-08-06 湖南大学 一种以碳材料催化氧化有机酮制备有机内酯的方法
CN102603447B (zh) * 2012-02-13 2014-09-03 湖南大学 一种制备有机内酯的方法
US8846984B2 (en) 2012-04-27 2014-09-30 E I Du Pont De Nemours And Company Production of α,ω-diols
US8859826B2 (en) 2012-04-27 2014-10-14 E I Du Pont De Nemours And Company Production of alpha, omega-diols
US9018423B2 (en) 2012-04-27 2015-04-28 E I Du Pont De Nemours And Company Production of alpha, omega-diols
US11208394B2 (en) 2018-09-17 2021-12-28 Regents Of The University Of Minnesota Chemical process to manufacture branched-caprolactone
GB202109710D0 (en) 2021-07-05 2021-08-18 Johnson Matthey Davy Technologies Ltd Separation process for the production of C5 or C6 alkanediol

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2819593A1 (de) * 1978-05-05 1979-11-08 Basf Ag Verfahren zur herstellung von diolen
EP0661255A1 (en) * 1993-12-28 1995-07-05 Ube Industries, Ltd. Process for producing diol compounds

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1618143C3 (de) * 1967-04-27 1975-08-21 Basf Ag, 6700 Ludwigshafen Verfahren zur Gewinnung von epsilon-Hydroxycapronsäurelacton und von Alkandicarbonsäuren
DE2060548C3 (de) * 1970-12-09 1979-10-11 Basf Ag, 6700 Ludwigshafen Verfahren zur Herstellung von sehr reinem 1,6-Hexandiol durch Kristallisation
DE2321101C2 (de) * 1973-04-26 1982-07-22 Basf Ag, 6700 Ludwigshafen Verfahren zur Herstellung im wesentlichen trägerfreier Kobaltkatalysatoren
US3933930A (en) * 1975-03-06 1976-01-20 Celanese Corporation Hexanediol from cyclohexane
DE3823213A1 (de) * 1988-07-08 1990-01-11 Basf Ag Verfahren zur herstellung von caprolacton
US5710349A (en) * 1993-10-08 1998-01-20 Ube Industries, Ltd. Process for producing diol compounds

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2819593A1 (de) * 1978-05-05 1979-11-08 Basf Ag Verfahren zur herstellung von diolen
EP0661255A1 (en) * 1993-12-28 1995-07-05 Ube Industries, Ltd. Process for producing diol compounds

Also Published As

Publication number Publication date
DE59701646D1 (de) 2000-06-15
KR100468182B1 (ko) 2005-03-16
PT883591E (pt) 2000-10-31
CA2248004C (en) 2006-04-11
JP2000506134A (ja) 2000-05-23
ES2147435T3 (es) 2000-09-01
CN1211969A (zh) 1999-03-24
MY118128A (en) 2004-09-30
US5981769A (en) 1999-11-09
EP0883591B1 (de) 2000-05-10
WO1997031883A1 (de) 1997-09-04
CA2248004A1 (en) 1997-09-04
KR19990087422A (ko) 1999-12-27
ATE192730T1 (de) 2000-05-15
JP4107396B2 (ja) 2008-06-25
EP0883591A1 (de) 1998-12-16
GR3033955T3 (en) 2000-11-30

Similar Documents

Publication Publication Date Title
CN1089742C (zh) 制备1,6-己二醇和己内酯的方法
JP5124366B2 (ja) 99%を越える純度を有する1,6−ヘキサンジオールの製法
US8471042B2 (en) Method for producing 1,6-hexanediol and caprolactone
US8629306B2 (en) Method for producing 1,6-hexanediol
CN101848904B (zh) 生产ε-己内酯的方法
US20120059174A1 (en) Process for preparing epsilon-caprolactone and 1,6-hexanediol
CN1906144A (zh) 制备1,6-己二醇的方法
CN1158234C (zh) 1,6-己二醇的制备方法
CN1659123A (zh) 丁二醇的制备方法
CN1668560A (zh) 带有琥珀酸酐中间去除的两步法制取丁二醇
US20110263907A1 (en) Process for preparing 1,6-hexanediol
RU2571082C2 (ru) СПОСОБ ПОЛУЧЕНИЯ ε-КАПРОЛАКТОНА И 1,6-ГЕКСАНДИОЛА
CN1253419C (zh) 己二醇的制备方法
CN1294110C (zh) 通过结合气相和液相氢化制备1,4-丁二醇的方法
CA2247991C (en) Process for preparing 1,6 hexane diol with a level of purity over 99 %

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
CX01 Expiry of patent term
CX01 Expiry of patent term

Granted publication date: 20020828