KR870700588A - 부탄-1,4-디올의 제조방법 - Google Patents

부탄-1,4-디올의 제조방법

Info

Publication number
KR870700588A
KR870700588A KR1019860700459A KR860700459A KR870700588A KR 870700588 A KR870700588 A KR 870700588A KR 1019860700459 A KR1019860700459 A KR 1019860700459A KR 860700459 A KR860700459 A KR 860700459A KR 870700588 A KR870700588 A KR 870700588A
Authority
KR
South Korea
Prior art keywords
diol
butane
preparing
preparing butane
Prior art date
Application number
KR1019860700459A
Other languages
English (en)
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 US06/673,797 external-priority patent/US4584419A/en
Priority claimed from PCT/GB1985/000524 external-priority patent/WO1986003189A1/en
Application filed filed Critical
Publication of KR870700588A publication Critical patent/KR870700588A/ko

Links

Classifications

    • 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
    • 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
    • C07C29/17Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrogenation of carbon-to-carbon double or triple bonds
    • C07C29/177Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrogenation of carbon-to-carbon double or triple bonds with simultaneous reduction of a carboxy group
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/04Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D307/06Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms
    • C07D307/08Preparation of tetrahydrofuran

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
KR1019860700459A 1984-11-21 1986-07-12 부탄-1,4-디올의 제조방법 KR870700588A (ko)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US06/673,797 US4584419A (en) 1983-11-29 1984-11-21 Process for the production of butane-1,4-diol
GB858514002A GB8514002D0 (en) 1985-06-04 1985-06-04 Process
PCT/GB1985/000524 WO1986003189A1 (en) 1984-11-21 1985-11-18 Process for the production of butane-1,4-diol

Publications (1)

Publication Number Publication Date
KR870700588A true KR870700588A (ko) 1987-12-30

Family

ID=10580110

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019860700459A KR870700588A (ko) 1984-11-21 1986-07-12 부탄-1,4-디올의 제조방법

Country Status (3)

Country Link
US (1) US4751334A (ko)
KR (1) KR870700588A (ko)
GB (1) GB8514002D0 (ko)

Families Citing this family (62)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0304696B1 (de) * 1987-08-08 1992-04-29 BASF Aktiengesellschaft Verfahren zur Herstellung von 1,4-Butandiol und/oder Tetrahydrofuran
JP2596604B2 (ja) * 1988-12-14 1997-04-02 東燃株式会社 1,4−ブタンジオールおよびテトラヒドロフランの製造方法
DE3843956A1 (de) * 1988-12-24 1990-06-28 Huels Chemische Werke Ag Verfahren zur herstellung von aliphatischen und cycloaliphatischen diolen durch katalytische hydrierung von dicarbonsaeureestern
JP2595358B2 (ja) * 1989-12-07 1997-04-02 東燃株式会社 1,4―ブタンジオールおよびテトラヒドロフランの製造方法
DE4005293A1 (de) * 1990-02-20 1991-08-22 Basf Ag Verfahren zur herstellung von tetrahydrofuran und -butyrolacton
US5030773A (en) * 1990-07-25 1991-07-09 General Electric Company Process for the production of butanediol
GB9324782D0 (en) * 1993-12-02 1994-01-19 Davy Mckee London Process
GB9324784D0 (en) * 1993-12-02 1994-01-19 Davy Mckee London Process
GB9324785D0 (en) * 1993-12-02 1994-01-19 Davy Mckee London Process
GB9324753D0 (en) * 1993-12-02 1994-01-19 Davy Mckee London Process
GB9324823D0 (en) * 1993-12-02 1994-01-19 Davy Mckee London Process
GB9324783D0 (en) * 1993-12-02 1994-01-19 Davy Mckee London Process
GB9324752D0 (en) * 1993-12-02 1994-01-19 Davy Mckee London Process
GB9324786D0 (en) * 1993-12-02 1994-01-19 Davy Mckee London Process
TW366335B (en) * 1996-03-29 1999-08-11 Kvaerner Process Tech Ltd Process for the purification of butane-1,4-diol
ZA973972B (en) * 1996-05-14 1998-03-23 Kvaerner Process Tech Ltd A process for the production of at least one C4 compound selected from butane-1,4-diol, gamma-butyrolactone and tetrahydrofuran.
GB9724004D0 (en) 1997-11-13 1998-10-21 Kvaerner Process Tech Ltd Process
BE1012342A6 (fr) 1998-01-08 2000-10-03 Pantochim Sa Procede de production de butanediol par hydrogenation en phase liquide.
BE1011698A6 (fr) 1998-01-08 1999-12-07 Pantochim Sa Procede de production de tetrahydrofuranne, de gamma-butyrolactone et de butanediol.
DE69800886T2 (de) 1998-03-23 2001-10-11 Basf Ag Verfahren zur Herstellung von 1,4-Butandiol, Butyrolacton und Tetrahydrofuran
US5883084A (en) * 1998-06-08 1999-03-16 Clarion Pharmaceuticals Inc. Treatment of respiratory diseases utilizing α-tocopheryl-phosphocholine
US6455742B1 (en) 1999-09-02 2002-09-24 Wisconsin Alumni Research Foundation Method for catalytically reducing carboxylic acid groups to hydroxyl groups in hydroxycarboxylic acids
GB0117090D0 (en) * 2001-07-12 2001-09-05 Kvaerner Process Tech Ltd Process
GB0325530D0 (en) * 2003-10-31 2003-12-03 Davy Process Techn Ltd Process
GB0421928D0 (en) * 2004-10-01 2004-11-03 Davy Process Techn Ltd Process
GB0803663D0 (en) * 2008-02-28 2008-04-09 Davy Process Techn Ltd Process
CN101747149B (zh) * 2008-12-11 2013-02-20 浙江杭州鑫富药业股份有限公司 一种马来酸二烷基酯两段法加氢制1,4-丁二醇的方法
US8575403B2 (en) 2010-05-07 2013-11-05 Celanese International Corporation Hydrolysis of ethyl acetate in ethanol separation process
WO2012148509A1 (en) 2011-04-26 2012-11-01 Celanese International Corporation Process for producing ethanol using a stacked bed reactor
US8859827B2 (en) 2011-11-18 2014-10-14 Celanese International Corporation Esterifying acetic acid to produce ester feed for hydrogenolysis
US8846988B2 (en) 2010-07-09 2014-09-30 Celanese International Corporation Liquid esterification for the production of alcohols
US8710279B2 (en) 2010-07-09 2014-04-29 Celanese International Corporation Hydrogenolysis of ethyl acetate in alcohol separation processes
US8664454B2 (en) 2010-07-09 2014-03-04 Celanese International Corporation Process for production of ethanol using a mixed feed using copper containing catalyst
US9272970B2 (en) 2010-07-09 2016-03-01 Celanese International Corporation Hydrogenolysis of ethyl acetate in alcohol separation processes
MY157438A (en) 2010-09-24 2016-06-15 Basf Se Process for the production of tetrahydrofuran
US9186599B2 (en) 2010-09-24 2015-11-17 Basf Se Process for isolating tetrahydrofuran
US8592635B2 (en) 2011-04-26 2013-11-26 Celanese International Corporation Integrated ethanol production by extracting halides from acetic acid
US9073816B2 (en) 2011-04-26 2015-07-07 Celanese International Corporation Reducing ethyl acetate concentration in recycle streams for ethanol production processes
US8907141B2 (en) 2011-04-26 2014-12-09 Celanese International Corporation Process to recover alcohol with secondary reactors for esterification of acid
US9000233B2 (en) 2011-04-26 2015-04-07 Celanese International Corporation Process to recover alcohol with secondary reactors for hydrolysis of acetal
US8754268B2 (en) 2011-04-26 2014-06-17 Celanese International Corporation Process for removing water from alcohol mixtures
CN102775274B (zh) * 2011-05-13 2015-01-21 中国石油化工集团公司 一种草酸酯加氢制乙二醇的系统及方法
US8895786B2 (en) 2011-08-03 2014-11-25 Celanese International Corporation Processes for increasing alcohol production
GB201115617D0 (en) 2011-09-09 2011-10-26 Davy Process Techn Ltd Proacess
US8829249B2 (en) 2011-11-18 2014-09-09 Celanese International Corporation Integrated esterification and hydrogenolysis process for producing ethanol
US9024089B2 (en) 2011-11-18 2015-05-05 Celanese International Corporation Esterification process using extractive separation to produce feed for hydrogenolysis
US8748673B2 (en) 2011-11-18 2014-06-10 Celanese International Corporation Process of recovery of ethanol from hydrogenolysis process
US8853468B2 (en) 2011-11-18 2014-10-07 Celanese International Corporation Vapor esterification method to produce ester feed for hydrogenolysis
US8829251B2 (en) 2011-11-18 2014-09-09 Celanese International Corporation Liquid esterification method to produce ester feed for hydrogenolysis
US8802901B2 (en) 2011-11-18 2014-08-12 Celanese International Corporation Continuous ethyl acetate production and hydrogenolysis thereof
EP2782893B1 (en) * 2011-11-25 2017-08-23 Conser SPA Process for producing 1,4-butanediol, gamma-butyrolactone and tetrahydrofuran by hydrogenating dialkyl maleate in mixed liquid/vapor phase
US8927790B2 (en) 2011-12-15 2015-01-06 Celanese International Corporation Multiple vapor feeds for hydrogenation process to produce alcohol
CN103804142B (zh) * 2012-11-07 2016-05-11 中国石油化工集团公司 一种草酸酯加氢制乙二醇的系统及方法
US8975451B2 (en) 2013-03-15 2015-03-10 Celanese International Corporation Single phase ester feed for hydrogenolysis
GB201318175D0 (en) 2013-10-14 2013-11-27 Johnson Matthey Davy Technologies Ltd Process
GB201321611D0 (en) 2013-12-06 2014-01-22 Johnson Matthey Davy Technologies Ltd Process
GB201321627D0 (en) 2013-12-06 2014-01-22 Johnson Matthey Davy Technologies Ltd Process
WO2016113758A1 (en) 2015-01-15 2016-07-21 Council Of Scientific & Industrial Research Catalytic hydrogenation process for the synthesis of terminal diols from terminal dialkyl aliphatic esters
GB201507234D0 (en) 2015-04-28 2015-06-10 Johnson Matthey Davy Technologies Ltd Process
KR20230156824A (ko) 2021-03-12 2023-11-14 꼰세르 엣세.삐.아. 2개의 스테이지들에서 디알킬 말리에이트를 수소화함으로써 디알킬 숙시네이트 및 1,4-부탄디올의 공생산을 위한 공정
CN114181038B (zh) 2021-12-24 2022-10-11 常州瑞华化工工程技术股份有限公司 一种顺酐直接加氢生产1,4-丁二醇并联产丁二酸酐的方法
GB202203264D0 (en) 2022-03-09 2022-04-20 Johnson Matthey Davy Technologies Ltd Process for producing a refined 1,4-butanediol stream

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2130501A (en) * 1934-06-27 1938-09-20 Du Pont Reduction of cyclic ethers
JPS4831084B1 (ko) * 1970-09-04 1973-09-26
US4032458A (en) * 1975-08-08 1977-06-28 Petro-Tex Chemical Corporation Production of 1,4-butanediol
US4112245A (en) * 1976-08-18 1978-09-05 Atlantic Richfield Company Process for the preparation of ethylene glycol
GB1587198A (en) * 1976-11-23 1981-04-01 Ucb Sa Process for the production of butane-1,4 diol and tetrahydrofuran
JPS57122940A (en) * 1981-01-26 1982-07-31 Ube Ind Ltd Hydrogenation catalyst of oxalic diester
GB8310797D0 (en) * 1983-04-21 1983-05-25 British Petroleum Co Plc Vapour phase hydrogenation of esters
GB8331793D0 (en) * 1983-11-29 1984-01-04 Davy Mckee Ltd Process

Also Published As

Publication number Publication date
GB8514002D0 (en) 1985-07-10
US4751334A (en) 1988-06-14

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Legal Events

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