AR017612A1 - Proceso para la preparacion de butano-1,4-diol, gamma-butirolactona y tetrahidrofurano - Google Patents

Proceso para la preparacion de butano-1,4-diol, gamma-butirolactona y tetrahidrofurano

Info

Publication number
AR017612A1
AR017612A1 ARP980105756A ARP980105756A AR017612A1 AR 017612 A1 AR017612 A1 AR 017612A1 AR P980105756 A ARP980105756 A AR P980105756A AR P980105756 A ARP980105756 A AR P980105756A AR 017612 A1 AR017612 A1 AR 017612A1
Authority
AR
Argentina
Prior art keywords
maleic anhydride
alkyl
esters
high boiling
hydrogenation
Prior art date
Application number
ARP980105756A
Other languages
English (en)
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 AR017612A1 publication Critical patent/AR017612A1/es

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

Un proceso para la preparacion de butano-1,4-diol, gamma-butirolactona y tetrahidrofurano, donde dicho proceso se lleva a cabo poniendo en contacto unacorriente vaporosa que contiene vapor de anhídrido maleico, vapor de agua y oxido de carbono en unazona de absorcion con un éster de alto punto deebullicion como solvente de manera de formar una solucion de anhídrido maleico en el éster de alto punto de ebullicion. El éster de alto punto deebullicion tiene un punto de ebullicion a presion atmosférica que es de por lo menos alrededor de 30*C más alto que aquél del anhídrido maleico y que estaseleccionado de los di-(C1-4 alquil) ésteres de los ácidos alquilo dicarboxílicos que contiene hasta 13 átomos de C, mono-di(C10-18 alquil) ésteres de ácidomaleico, ácido fumárico, ácido succínico y mezclas de los mismos C1-4 alquil) ésteres de ácidos aromáticos tricarboxílicos, y di-(C1-4 alquil) ésteresde ácido isoftálico. Una corriente de gas de desecho es recuperada de la zona de absorcion. La solucion de anhídrido maleico en el éster de alto puntode ebullicion es puesto en contacto con una corriente gaseosa que contiene hidrogeno de manera de desprender anhídrido maleico del mismo y deformaruna corriente vaporosa que contiene hidrogeno y anhídrido maleico. Material de esta corriente vaporosa es puesto en contacto con una zona de hidrogenacionbajo condiciones de hidrogenacion con un catalizador de hidrogenacion heterogénea de manera de convertir el anhídrido maleico por hidrogenacion enal menos uncompuesto C4 seleccionado de butano-1,4-diol, gamma-butirolactona y tetrahidrofurano y una corriente de producto que contiene dicho por lo menos un compuestoC4 se recupera de la zona de hidrogenacion.
ARP980105756A 1997-11-14 1998-11-13 Proceso para la preparacion de butano-1,4-diol, gamma-butirolactona y tetrahidrofurano AR017612A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB9724195.4A GB9724195D0 (en) 1997-11-14 1997-11-14 Process

Publications (1)

Publication Number Publication Date
AR017612A1 true AR017612A1 (es) 2001-09-12

Family

ID=10822149

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP980105756A AR017612A1 (es) 1997-11-14 1998-11-13 Proceso para la preparacion de butano-1,4-diol, gamma-butirolactona y tetrahidrofurano

Country Status (20)

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

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
BR112013031703B1 (pt) 2011-06-09 2019-04-02 Micromidas, Inc. Método para a produção de um furano substituído em um reator multifásico.
KR20150072453A (ko) 2012-10-26 2015-06-29 마이크로마이다스, 인코포레이티드 5-(할로메틸) 푸르푸랄 생산 방법
MY193787A (en) 2013-03-14 2022-10-27 Micromidas Inc Solid forms of 5-(halomethyl) furfural and methods for preparing thereof
MX2015012878A (es) 2013-03-14 2016-02-03 Micromidas Inc Metodos para purificar 5-(halometil)furfural.
EP4166546A1 (en) 2013-09-20 2023-04-19 Origin Materials Operating, 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)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
BE547079A (es) 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
US4118403A (en) 1976-11-18 1978-10-03 Monsanto Company Recovery of maleic anhydride
GB8331793D0 (en) 1983-11-29 1984-01-04 Davy Mckee Ltd Process
EP0204730A1 (en) 1984-11-21 1986-12-17 DAVY McKEE (LONDON) LIMITED Process for the production of butane-1,4-diol
EP0277168A1 (en) 1986-08-01 1988-08-10 DAVY McKEE (LONDON) LIMITED PROCESS FOR THE CO-PRODUCTION OF BUTANE-1,4-DIOL AND $i(GAMMA)-BUTYROLACTONE
GB8618890D0 (en) 1986-08-01 1986-09-10 Davy Mckee Ltd Process
GB8717993D0 (en) 1987-07-29 1987-09-03 Davy Mckee Ltd Process
GB8717992D0 (en) 1987-07-29 1987-09-03 Davy Mckee Ltd Process
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
GB8917859D0 (en) 1989-08-04 1989-09-20 Davy Mckee London Process
GB8917862D0 (en) 1989-08-04 1989-09-20 Davy Mckee London Process
GB8917864D0 (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
US5631387A (en) * 1995-03-20 1997-05-20 Huntsman Petrochemical Corporation Process for the preparation and recovery of maleic anhydride
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
NO20002472L (no) 2000-05-12
US6204395B1 (en) 2001-03-20
TW460444B (en) 2001-10-21
CA2309992A1 (en) 1999-05-27
CN1281424A (zh) 2001-01-24
ZA989584B (en) 1999-08-25
ES2195406T3 (es) 2003-12-01
NO20002472D0 (no) 2000-05-12
WO1999025675A1 (en) 1999-05-27
CN1132805C (zh) 2003-12-31
DE69812429D1 (de) 2003-04-24
BR9814141A (pt) 2000-10-03
AU9753398A (en) 1999-06-07
AU761294B2 (en) 2003-05-29
MY118197A (en) 2004-09-30
SA99191004B1 (ar) 2006-10-04
JP2001523656A (ja) 2001-11-27
KR100530781B1 (ko) 2005-11-23
GB9724195D0 (en) 1998-01-14
EP1049657A1 (en) 2000-11-08
EP1049657B1 (en) 2003-03-19
DE69812429T2 (de) 2003-08-14
KR20010032013A (ko) 2001-04-16
ID26660A (id) 2001-01-25
JP4268335B2 (ja) 2009-05-27
MXPA00004661A (es) 2003-08-20

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