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BR9814141A - Processo para a preparação de butano-1,4-diol, gama-butiro-lactona e tetraidrofurano - Google Patents

Processo para a preparação de butano-1,4-diol, gama-butiro-lactona e tetraidrofurano

Info

Publication number
BR9814141A
BR9814141A BR9814141-4A BR9814141A BR9814141A BR 9814141 A BR9814141 A BR 9814141A BR 9814141 A BR9814141 A BR 9814141A BR 9814141 A BR9814141 A BR 9814141A
Authority
BR
Brazil
Prior art keywords
alkyl
maleic anhydride
esters
butane
diol
Prior art date
Application number
BR9814141-4A
Other languages
English (en)
Inventor
Michael William Marshall Tuck
Michael Anthony Wood
Andrew George Hiles
Original Assignee
Basf Ag
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 Basf Ag filed Critical Basf Ag
Publication of BR9814141A publication Critical patent/BR9814141A/pt

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D315/00—Heterocyclic compounds containing rings having one oxygen atom as the only ring hetero atom according to more than one of groups C07D303/00 - C07D313/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/26—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D307/30—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D307/32—Oxygen atoms
    • C07D307/33—Oxygen atoms in position 2, the oxygen atom being in its keto or unsubstituted enol form
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/132—Preparation 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
    • C07C29/136—Preparation 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
    • C07C29/147—Preparation 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
    • C07C29/149—Preparation 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C31/00—Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C31/18—Polyhydroxylic acyclic alcohols
    • C07C31/20—Dihydroxylic alcohols
    • C07C31/207—1,4-Butanediol; 1,3-Butanediol; 1,2-Butanediol; 2,3-Butanediol
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/04—Heterocyclic 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
    • C07D307/06—Heterocyclic 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
    • C07D307/08—Preparation of tetrahydrofuran

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Furan Compounds (AREA)

Abstract

Patente de Invenção: <B>"PROCESSO PARA A PREPARAçãO DE BUTANO-1,4-DIOL, GAMA-BUTIROLACTONA E TETRAIDROFURANO"<D>. é descrito um processo para a produção de butano-1,4-diol, <sym>-butirolactona e/ou tetraidrofurano. Uma corrente de vapor contendo anidrido maléico, água e óxidos de carbono é posta em contato em uma zona de absorção com um éster de alta ebulição como solvente para formar uma solução de anidrido maléico no éster de alta ebulição, que tenha um ponto de ebulição na pressão atmosférica de pelo menos cerca de 30° C acima do de anidrido maléico e que seja selecionada de di-(C~ 1~ a C~ 4~ alquil)ésteres de ácidos dicarboxílicos de alquila contendo até 13 átomos de carbono, mono- e di-(C~ 10~ a C~ 18~ alquil)ésteres de ácido maléico, ácido fumárico, ácido succínico e suas misturas, (C~ 1~ a C~ 4~ alquil)ésteres de ácidos naflateno-carboxílicos, tri (C~ 1~ a C~ 4~ alquil)ésteres de ácidos tricarboxílicos aromáticos e di-(C~ 1~ a C~ 4~ alquil)ésteres de ácido isoftálico. O anidrido maléico na solução é retirado com uma corrente gasosa contendo hidrogênio. daí formando uma corrente de vapor compreendendo hidrogênio e anidrido maléico que é posto em contato em uma zona de hidrogenação com um catalisador de hidrogenação heterogêneo para converter o anidrido maléico em pelo menos um composto C~ 4~ selecionado de butano-1,4-diol, <sym>-butirolactona e tetraidrofurano.
BR9814141-4A 1997-11-14 1998-11-02 Processo para a preparação de butano-1,4-diol, gama-butiro-lactona e tetraidrofurano BR9814141A (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB9724195.4A GB9724195D0 (en) 1997-11-14 1997-11-14 Process
PCT/GB1998/003257 WO1999025675A1 (en) 1997-11-14 1998-11-02 Process for the preparation of butane-1,4-diol, gamma-butyrolactone and tetrahydrofuran

Publications (1)

Publication Number Publication Date
BR9814141A true BR9814141A (pt) 2000-10-03

Family

ID=10822149

Family Applications (1)

Application Number Title Priority Date Filing Date
BR9814141-4A BR9814141A (pt) 1997-11-14 1998-11-02 Processo para a preparação de butano-1,4-diol, gama-butiro-lactona e tetraidrofurano

Country Status (20)

Country Link
US (1) US6204395B1 (pt)
EP (1) EP1049657B1 (pt)
JP (1) JP4268335B2 (pt)
KR (1) KR100530781B1 (pt)
CN (1) CN1132805C (pt)
AR (1) AR017612A1 (pt)
AU (1) AU761294B2 (pt)
BR (1) BR9814141A (pt)
CA (1) CA2309992A1 (pt)
DE (1) DE69812429T2 (pt)
ES (1) ES2195406T3 (pt)
GB (1) GB9724195D0 (pt)
ID (1) ID26660A (pt)
MX (1) MXPA00004661A (pt)
MY (1) MY118197A (pt)
NO (1) NO20002472D0 (pt)
SA (1) SA99191004B1 (pt)
TW (1) TW460444B (pt)
WO (1) WO1999025675A1 (pt)
ZA (1) ZA989584B (pt)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19818340A1 (de) * 1998-04-23 1999-10-28 Basf Ag Verfahren zur Herstellung von Gemischen aus 1,4-Butandiol, Tetrahydrofuran und gamma-Butyrolacton
DE10219224A1 (de) * 2002-04-30 2003-11-13 Basf Ag Verfahren zur Herstellung von gamma-Butyrolacton
GB0325526D0 (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
MY184015A (en) 2011-06-09 2021-03-17 Micromidas Inc Utilizing a multiphase reactor for the conversion of biomass to produce substituted furans
JP2015533851A (ja) 2012-10-26 2015-11-26 マイクロマイダス，インコーポレイテッド ５−（ハロメチル）フルフラールの生成方法
MX2015011732A (es) 2013-03-14 2015-12-01 Micromidas Inc Formas solidas de 5-(halometil)furfural y metodos para preparar las mismas.
JP2016514145A (ja) * 2013-03-14 2016-05-19 マイクロマイダス，インコーポレイテッド ５−（ハロメチル）フルフラールの精製方法
US10011577B2 (en) 2013-09-20 2018-07-03 Micromidas, Inc. Methods for producing 5-(halomethyl)furfural
US20240287011A1 (en) * 2021-06-25 2024-08-29 Cj Cheiljedang Corporation Method for producing tetrahydrofuran, gamma-butyrolactone, or 1,4-butanediol
KR102604948B1 (ko) * 2021-06-25 2023-11-23 씨제이제일제당(주) 테트라하이드로퓨란, 감마부티로락톤 또는 1,4-부탄디올의 제조 방법

Family Cites Families (27)

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US2638481A (en) 1950-05-26 1953-05-12 Hercules Powder Co Ltd Maleic acid manufacture
GB727828A (en) 1952-12-09 1955-04-06 Chempatents Inc Recovery of polycarboxylic acid anhydrides
GB763339A (en) 1953-03-23 1956-12-12 Chempatents Inc Improvements in recovery of maleic and phthalic acid anhydrides
FR1089012A (fr) 1953-10-08 1955-03-14 Chempatents Procédé de récupération des anhydrides d'acides polycarboxyliques à partir de mélanges gazeux dilués
NL98195C (pt) 1955-04-20
US2893924A (en) 1956-04-17 1959-07-07 Saint Gobain Separation and purification of anhydrides of organic diacids
US3040059A (en) 1959-07-02 1962-06-19 Foster Wheeler Corp Recovery of the anhydrides of polycarboxylic acids
BE792879A (fr) 1971-12-17 1973-03-30 Chevron Res Procede d'isolement de l'anhydride maleique
US3891680A (en) 1972-11-29 1975-06-24 Chevron Res Maleic anhydride recovery using nonaqueous medium
US3850758A (en) 1973-07-02 1974-11-26 Allied Chem Purification of crude maleic anhydride by treatment with dimethylbenzophenone
DE2444824A1 (de) 1974-09-19 1976-04-08 Basf Ag Verfahren zur gewinnung von maleinsaeureanhydrid
US4071540A (en) 1976-07-08 1978-01-31 Chevron Research Company Anhydride separation process
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GB8331793D0 (en) 1983-11-29 1984-01-04 Davy Mckee Ltd Process
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WO1988000937A1 (en) 1986-08-01 1988-02-11 Davy Mckee (London) Limited Process for the co-production of butane-1,4-diol and gamma-butyrolactone
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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
GB8917864D0 (en) 1989-08-04 1989-09-20 Davy Mckee London Process
GB8917859D0 (en) 1989-08-04 1989-09-20 Davy Mckee London Process
GB8917862D0 (en) 1989-08-04 1989-09-20 Davy Mckee London Process
US5347021A (en) 1990-04-16 1994-09-13 Isp Investments Inc. Process of vapor phase catalytic hydrogenation of maleic anhydride to gamma-butyrolactone in high conversion and high selectivity using an activated catalyst
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ZA973971B (en) 1996-05-15 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.
US5869700A (en) 1997-02-21 1999-02-09 Exxon Chemical Patents Inc. Method for recovering phthalic anhydride/maleic anhydride mixtures by distillation

Also Published As

Publication number Publication date
CN1281424A (zh) 2001-01-24
WO1999025675A1 (en) 1999-05-27
AU9753398A (en) 1999-06-07
US6204395B1 (en) 2001-03-20
SA99191004B1 (ar) 2006-10-04
ID26660A (id) 2001-01-25
DE69812429D1 (de) 2003-04-24
KR100530781B1 (ko) 2005-11-23
EP1049657B1 (en) 2003-03-19
CA2309992A1 (en) 1999-05-27
AR017612A1 (es) 2001-09-12
EP1049657A1 (en) 2000-11-08
GB9724195D0 (en) 1998-01-14
TW460444B (en) 2001-10-21
JP2001523656A (ja) 2001-11-27
DE69812429T2 (de) 2003-08-14
AU761294B2 (en) 2003-05-29
ZA989584B (en) 1999-08-25
JP4268335B2 (ja) 2009-05-27
MY118197A (en) 2004-09-30
CN1132805C (zh) 2003-12-31
NO20002472L (no) 2000-05-12
ES2195406T3 (es) 2003-12-01
NO20002472D0 (no) 2000-05-12
MXPA00004661A (es) 2003-08-20
KR20010032013A (ko) 2001-04-16

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Legal Events

Date Code Title Description
B08F Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette]

Free format text: REFERENTE AO NAO RECOLHIMENTO DA 10A ANUIDADE.

B08K Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette]

Free format text: REFERENTE AO DESPACHO 8.6 DA RPI 1986 DE 27/03/2009.