TW275627B - - Google Patents

Info

Publication number
TW275627B
TW275627B TW081109243A TW81109243A TW275627B TW 275627 B TW275627 B TW 275627B TW 081109243 A TW081109243 A TW 081109243A TW 81109243 A TW81109243 A TW 81109243A TW 275627 B TW275627 B TW 275627B
Authority
TW
Taiwan
Prior art keywords
epoxyalkenes
delta
gamma
dihydrofurans
isomerization
Prior art date
Application number
TW081109243A
Other languages
English (en)
Chinese (zh)
Original Assignee
Eastman Chem 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 Chem Co filed Critical Eastman Chem Co
Application granted granted Critical
Publication of TW275627B publication Critical patent/TW275627B/zh

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)
TW081109243A 1991-11-19 1992-11-18 TW275627B (enExample)

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
TW275627B true TW275627B (enExample) 1996-05-11

Family

ID=27114936

Family Applications (1)

Application Number Title Priority Date Filing Date
TW081109243A TW275627B (enExample) 1991-11-19 1992-11-18

Country Status (16)

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

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
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
US6472491B1 (en) 2000-10-05 2002-10-29 Eastman Chemical Company Process for preparing ethylene interpolymers 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
CN101448807B (zh) * 2006-03-17 2013-02-06 康奈尔大学 2,5-二氢呋喃及类似化合物的制备

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
ATE149492T1 (de) 1997-03-15
JP3184527B2 (ja) 2001-07-09
DE69217999D1 (de) 1997-04-10
MY108257A (en) 1996-08-30
AU665502B2 (en) 1996-01-04
AU3131693A (en) 1993-06-15
GR3022904T3 (en) 1997-06-30
CA2122455A1 (en) 1993-05-27
DK0624157T3 (da) 1997-09-15
EP0624157A1 (en) 1994-11-17
DE69217999T2 (de) 1997-06-12
ES2098562T3 (es) 1997-05-01
EP0624157B1 (en) 1997-03-05
CA2122455C (en) 1997-12-09
CN1050837C (zh) 2000-03-29
WO1993010111A1 (en) 1993-05-27
CN1073435A (zh) 1993-06-23
US5315019A (en) 1994-05-24
BR9206778A (pt) 1995-11-07
JPH07507043A (ja) 1995-08-03
KR100222119B1 (ko) 1999-10-01

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