ES2098562T3 - Procedimiento continuo para la produccion de 2,5-dihidrofuranos a partir de gamma,delta-epoxibutenos. - Google Patents

Procedimiento continuo para la produccion de 2,5-dihidrofuranos a partir de gamma,delta-epoxibutenos.

Info

Publication number
ES2098562T3
ES2098562T3 ES92925142T ES92925142T ES2098562T3 ES 2098562 T3 ES2098562 T3 ES 2098562T3 ES 92925142 T ES92925142 T ES 92925142T ES 92925142 T ES92925142 T ES 92925142T ES 2098562 T3 ES2098562 T3 ES 2098562T3
Authority
ES
Spain
Prior art keywords
epoxibutenos
dihidrofuranes
delta
gamma
production
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
ES92925142T
Other languages
English (en)
Inventor
Gerald Wayne Phillips
Stephen Neal Falling
Stephen Allen Godleski
John Robert Monnier
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.)
Eastman Chemical Co
Original Assignee
Eastman Chemical Co
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 Eastman Chemical Co filed Critical Eastman Chemical Co
Application granted granted Critical
Publication of ES2098562T3 publication Critical patent/ES2098562T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • C07D307/28—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 only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/06—Halogens; Compounds thereof
    • B01J27/08—Halides
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0234—Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
    • B01J31/0235—Nitrogen containing compounds
    • B01J31/0239—Quaternary ammonium compounds
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0234—Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
    • B01J31/0255—Phosphorus containing compounds
    • B01J31/0267—Phosphines or phosphonium compounds, i.e. phosphorus bonded to at least one carbon atom, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, the other atoms bonded to phosphorus being either carbon or hydrogen
    • B01J31/0268—Phosphonium compounds, i.e. phosphine with an additional hydrogen or carbon atom bonded to phosphorous so as to result in a formal positive charge on phosphorous
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/12—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
    • B01J31/122—Metal aryl or alkyl compounds
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/50—Redistribution or isomerisation reactions of C-C, C=C or C-C triple bonds
    • B01J2231/52—Isomerisation reactions

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Catalysts (AREA)
  • Saccharide Compounds (AREA)
  • Epoxy Resins (AREA)
  • Epoxy Compounds (AREA)

Abstract

SE DESCRIBE UN PROCESO CONTINUO PARA LA FABRICACION DE DIHIDROFURANOS DELTA EN FASE LIQUIDA EN PRESENCIA DE UN SISTEMA CATALITICO QUE COMPRENDE UN COMPUESTO DE YODURO DE ONIO Y UN ACIDO LEWIS Y UN PROCESO DISOLVENTE QUE COMPRENDE UNA MEZCLA DEL PRODUCTO DIHIDROFURANO EPOXIALQUENOS - GAMMA, DELTA.
ES92925142T 1991-11-19 1992-11-09 Procedimiento continuo para la produccion de 2,5-dihidrofuranos a partir de gamma,delta-epoxibutenos. Expired - Lifetime ES2098562T3 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US74840891A 1991-11-19 1991-11-19
US07/962,545 US5315019A (en) 1991-11-19 1992-10-19 Continuous process for the manufacture of 2,5-dihydrofurans from γ, δ-epoxybutenes

Publications (1)

Publication Number Publication Date
ES2098562T3 true ES2098562T3 (es) 1997-05-01

Family

ID=27114936

Family Applications (1)

Application Number Title Priority Date Filing Date
ES92925142T Expired - Lifetime ES2098562T3 (es) 1991-11-19 1992-11-09 Procedimiento continuo para la produccion de 2,5-dihidrofuranos a partir de gamma,delta-epoxibutenos.

Country Status (16)

Country Link
US (1) US5315019A (es)
EP (1) EP0624157B1 (es)
JP (1) JP3184527B2 (es)
KR (1) KR100222119B1 (es)
CN (1) CN1050837C (es)
AT (1) ATE149492T1 (es)
AU (1) AU665502B2 (es)
BR (1) BR9206778A (es)
CA (1) CA2122455C (es)
DE (1) DE69217999T2 (es)
DK (1) DK0624157T3 (es)
ES (1) ES2098562T3 (es)
GR (1) GR3022904T3 (es)
MY (1) MY108257A (es)
TW (1) TW275627B (es)
WO (1) WO1993010111A1 (es)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0740676B1 (en) * 1994-01-18 1998-08-12 Eastman Chemical Company Polyether polymers derived from 3,4-epoxy-1-butene
DE4422671A1 (de) 1994-06-30 1996-01-04 Basf Ag Verfahren zur Herstellung von 2,5-Dihydrofuran
DE4424219A1 (de) * 1994-07-09 1996-01-11 Basf Ag Verfahren zur Herstellung von 2,5-Dihydrofuran
US5466832A (en) * 1995-02-13 1995-11-14 Eastman Chemical Company Process for the manufacture of 2,5-dihydrofurans from γ, δ-epoxybutenes
US5591874A (en) * 1995-09-29 1997-01-07 Eastman Chemical Company Process for the preparation of 2,5-dihydrofuran compounds
DE19539331A1 (de) * 1995-10-23 1997-04-24 Basf Ag Verfahren zur Abtrennung von oligomeren Nebenprodukten von einem Isomerisierungskatalysator
US5681969A (en) * 1996-05-03 1997-10-28 Eastman Chemical Company Continuous process for the conversion of 2,5-dihydrofuran to 2,3-dihydrofuran
US5693833A (en) * 1996-08-26 1997-12-02 Eastman Chemical Company Process for the reactivation of iodine-containing catalysts
US6090900A (en) * 1997-02-25 2000-07-18 Eastman Chemical Company Polymers containing functionalized olefin monomers
US6335455B1 (en) * 1998-01-12 2002-01-01 Eastman Chemical Company Process for the production of 2,5-dihydrofuran
US5986141A (en) * 1998-09-29 1999-11-16 Eastman Chemical Company Process for the production of cyclopropanemethylamine
US6472491B1 (en) 2000-10-05 2002-10-29 Eastman Chemical Company Process for preparing ethylene interpolymers and ethylene interpolymers
US6608156B1 (en) 2000-10-05 2003-08-19 Eastman Chemical Company Process for preparing interpolymers of ethylene and 2,3-dihydrofuran, or a heteroatom substituted olefin monomer and ethylene interpolymers
US6353140B1 (en) 2000-10-19 2002-03-05 Eastman Chemical Company Process for the purification of cyclopropanecarboxaldehyde
US7001369B2 (en) * 2003-03-27 2006-02-21 Scimed Life Systems, Inc. Medical device
US8404872B2 (en) * 2006-03-17 2013-03-26 Cornell University Production of 2,5-dihydrofurans and analogous compounds

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3812158A (en) * 1970-12-17 1974-05-21 Petro Tex Chem Corp Preparation of dihydrofuran from 3,4-epoxy-1-butene,3,4-dihydroxy-1-butene,or 1,4-dihydroxy-2-butene
US3932468A (en) * 1974-02-08 1976-01-13 Chevron Research Company Dihydrofuran preparation
US3996248A (en) * 1975-11-17 1976-12-07 Chevron Research Company Preparation of 2,5-dihydrofurans from butadiene monoxides
DE3926147A1 (de) * 1989-08-08 1991-02-14 Basf Ag Verfahren zur herstellung von 2,5-dihydrofuranen
US5082956A (en) * 1990-03-08 1992-01-21 Eastman Kodak Company Isomerization of epoxyalkenes to 2,5-dihydrofurans

Also Published As

Publication number Publication date
CN1073435A (zh) 1993-06-23
KR100222119B1 (ko) 1999-10-01
EP0624157A1 (en) 1994-11-17
CA2122455C (en) 1997-12-09
US5315019A (en) 1994-05-24
CN1050837C (zh) 2000-03-29
CA2122455A1 (en) 1993-05-27
WO1993010111A1 (en) 1993-05-27
JP3184527B2 (ja) 2001-07-09
TW275627B (es) 1996-05-11
DK0624157T3 (da) 1997-09-15
AU3131693A (en) 1993-06-15
AU665502B2 (en) 1996-01-04
JPH07507043A (ja) 1995-08-03
BR9206778A (pt) 1995-11-07
EP0624157B1 (en) 1997-03-05
ATE149492T1 (de) 1997-03-15
GR3022904T3 (en) 1997-06-30
MY108257A (en) 1996-08-30
DE69217999T2 (de) 1997-06-12
DE69217999D1 (de) 1997-04-10

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