KR100222119B1 - 감마,델타-에폭시부텐으로부터 2,5-디하이드로푸란을 제조하는 연속공정 - Google Patents

감마,델타-에폭시부텐으로부터 2,5-디하이드로푸란을 제조하는 연속공정 Download PDF

Info

Publication number
KR100222119B1
KR100222119B1 KR1019940701687A KR19940701687A KR100222119B1 KR 100222119 B1 KR100222119 B1 KR 100222119B1 KR 1019940701687 A KR1019940701687 A KR 1019940701687A KR 19940701687 A KR19940701687 A KR 19940701687A KR 100222119 B1 KR100222119 B1 KR 100222119B1
Authority
KR
South Korea
Prior art keywords
iodide
reaction zone
alkyl
dihydrofuran
compounds
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 - Fee Related
Application number
KR1019940701687A
Other languages
English (en)
Korean (ko)
Inventor
제럴드 웨인 필립스
스테펀 닐 폴링
스테펀 알렌 굿러스키
존 로버트 모니어
Original Assignee
그윈넬 해리 제이
이스트만 케미칼 컴퍼니
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 그윈넬 해리 제이, 이스트만 케미칼 컴퍼니 filed Critical 그윈넬 해리 제이
Application granted granted Critical
Publication of KR100222119B1 publication Critical patent/KR100222119B1/ko
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • 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
    • C07D307/26Heterocyclic 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
    • C07D307/28Heterocyclic 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J27/00Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/06Halogens; Compounds thereof
    • B01J27/08Halides
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0234Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
    • B01J31/0235Nitrogen containing compounds
    • B01J31/0239Quaternary ammonium compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0234Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
    • B01J31/0255Phosphorus containing compounds
    • B01J31/0267Phosphines 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
    • B01J31/0268Phosphonium 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/12Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
    • B01J31/122Metal aryl or alkyl compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/50Redistribution or isomerisation reactions of C-C, C=C or C-C triple bonds
    • B01J2231/52Isomerisation 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 Compounds (AREA)
  • Epoxy Resins (AREA)
KR1019940701687A 1991-11-19 1992-11-09 감마,델타-에폭시부텐으로부터 2,5-디하이드로푸란을 제조하는 연속공정 Expired - Fee Related KR100222119B1 (ko)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US74840891A 1991-11-19 1991-11-19
US748408 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
PCT/US1992/009676 WO1993010111A1 (en) 1991-11-19 1992-11-09 CONTINUOUS PROCESS FOR THE MANUFACTURE OF 2,5-DIHYDROFURANS FROM η,δ-EPOXYBUTENES
US962545 1997-10-31

Publications (1)

Publication Number Publication Date
KR100222119B1 true KR100222119B1 (ko) 1999-10-01

Family

ID=27114936

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019940701687A Expired - Fee Related KR100222119B1 (ko) 1991-11-19 1992-11-09 감마,델타-에폭시부텐으로부터 2,5-디하이드로푸란을 제조하는 연속공정

Country Status (16)

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

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2119392T3 (es) * 1994-01-18 1998-10-01 Eastman Chem Co Polimeros polieter derivados de 3,4-epoxi-1-buteno.
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
WO1998037110A1 (en) * 1997-02-25 1998-08-27 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
EP0624157B1 (en) 1997-03-05
CN1073435A (zh) 1993-06-23
TW275627B (https=) 1996-05-11
DE69217999D1 (de) 1997-04-10
GR3022904T3 (en) 1997-06-30
CN1050837C (zh) 2000-03-29
JP3184527B2 (ja) 2001-07-09
DK0624157T3 (da) 1997-09-15
MY108257A (en) 1996-08-30
CA2122455A1 (en) 1993-05-27
ATE149492T1 (de) 1997-03-15
ES2098562T3 (es) 1997-05-01
CA2122455C (en) 1997-12-09
DE69217999T2 (de) 1997-06-12
AU665502B2 (en) 1996-01-04
US5315019A (en) 1994-05-24
AU3131693A (en) 1993-06-15
EP0624157A1 (en) 1994-11-17
WO1993010111A1 (en) 1993-05-27
JPH07507043A (ja) 1995-08-03
BR9206778A (pt) 1995-11-07

Similar Documents

Publication Publication Date Title
KR100222119B1 (ko) 감마,델타-에폭시부텐으로부터 2,5-디하이드로푸란을 제조하는 연속공정
US6342614B1 (en) Isomerization of epoxyalkenes to 2,5-dihydrofurans
CN101522697A (zh) 二烷基锡二醇盐的制造方法
GB2034307A (en) Preparation of 1,1-diesters
KR100219872B1 (ko) 촉매혼합물로부터올리고머물질을분리하는방법
JP4574351B2 (ja) オルガノジアルキルアルコキシシランの製造方法
US6335455B1 (en) Process for the production of 2,5-dihydrofuran
JP4402117B2 (ja) オルガノアルコキシジアルキルシランの製造方法
US6201138B1 (en) Isomerization of epoxyalkenes to 2,5-dihydrofurans
US6462214B1 (en) Method of preparing silacycloalkanes
US6096673A (en) Catalyst recovery in the production of 2,5-dihydrofuran by isomerization of vinyl oxirane
US4328362A (en) Conversion of acetic anhydride to ethylidene diacetate
KR20000035812A (ko) 요오드 함유 촉매의 재활성화 방법
JP2908055B2 (ja) 1,4−ブタンジオ−ルの製造法

Legal Events

Date Code Title Description
PA0105 International application

St.27 status event code: A-0-1-A10-A15-nap-PA0105

R17-X000 Change to representative recorded

St.27 status event code: A-3-3-R10-R17-oth-X000

PG1501 Laying open of application

St.27 status event code: A-1-1-Q10-Q12-nap-PG1501

N231 Notification of change of applicant
PN2301 Change of applicant

St.27 status event code: A-3-3-R10-R13-asn-PN2301

St.27 status event code: A-3-3-R10-R11-asn-PN2301

A201 Request for examination
PA0201 Request for examination

St.27 status event code: A-1-2-D10-D11-exm-PA0201

PN2301 Change of applicant

St.27 status event code: A-3-3-R10-R13-asn-PN2301

St.27 status event code: A-3-3-R10-R11-asn-PN2301

E701 Decision to grant or registration of patent right
PE0701 Decision of registration

St.27 status event code: A-1-2-D10-D22-exm-PE0701

GRNT Written decision to grant
PR0701 Registration of establishment

St.27 status event code: A-2-4-F10-F11-exm-PR0701

PR1002 Payment of registration fee

St.27 status event code: A-2-2-U10-U12-oth-PR1002

Fee payment year number: 1

R17-X000 Change to representative recorded

St.27 status event code: A-5-5-R10-R17-oth-X000

PG1601 Publication of registration

St.27 status event code: A-4-4-Q10-Q13-nap-PG1601

LAPS Lapse due to unpaid annual fee
PC1903 Unpaid annual fee

St.27 status event code: A-4-4-U10-U13-oth-PC1903

Not in force date: 20020703

Payment event data comment text: Termination Category : DEFAULT_OF_REGISTRATION_FEE

PC1903 Unpaid annual fee

St.27 status event code: N-4-6-H10-H13-oth-PC1903

Ip right cessation event data comment text: Termination Category : DEFAULT_OF_REGISTRATION_FEE

Not in force date: 20020703

R18-X000 Changes to party contact information recorded

St.27 status event code: A-5-5-R10-R18-oth-X000

P22-X000 Classification modified

St.27 status event code: A-4-4-P10-P22-nap-X000