ES2132621T3 - Metodo para producir diolefinas trans no conjugadas. - Google Patents

Metodo para producir diolefinas trans no conjugadas.

Info

Publication number
ES2132621T3
ES2132621T3 ES95906139T ES95906139T ES2132621T3 ES 2132621 T3 ES2132621 T3 ES 2132621T3 ES 95906139 T ES95906139 T ES 95906139T ES 95906139 T ES95906139 T ES 95906139T ES 2132621 T3 ES2132621 T3 ES 2132621T3
Authority
ES
Spain
Prior art keywords
trans
conjugated diolefins
unjugged
olephine
hexadiene
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
ES95906139T
Other languages
English (en)
Inventor
Robert Scott Smith
Jos Peter Wristers
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.)
ExxonMobil Chemical Patents Inc
Original Assignee
Exxon Chemical Patents Inc
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 Exxon Chemical Patents Inc filed Critical Exxon Chemical Patents Inc
Application granted granted Critical
Publication of ES2132621T3 publication Critical patent/ES2132621T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C6/00—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions
    • C07C6/02—Metathesis reactions at an unsaturated carbon-to-carbon bond
    • C07C6/04—Metathesis reactions at an unsaturated carbon-to-carbon bond at a carbon-to-carbon double bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • C07C2523/24—Chromium, molybdenum or tungsten
    • C07C2523/28—Molybdenum
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • C07C2523/24—Chromium, molybdenum or tungsten
    • C07C2523/30—Tungsten
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • C07C2523/32—Manganese, technetium or rhenium
    • C07C2523/36—Rhenium
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper
    • C07C2523/74—Iron group metals
    • C07C2523/75—Cobalt
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • C07C2531/12—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
    • C07C2531/14—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/582—Recycling of unreacted starting or intermediate materials

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Catalysts (AREA)

Abstract

SE SUMINISTRA UN METODO PARA PRODUCIR SELECTIVAMENTE UN ISOMERO TRANS-GEOMETRICO DE DIOLEFINAS NO CONJUGADAS. EL METODO COMPRENDE EL TRATAMIENTO DE UN ISOMERO DE DIOLEFINA NO CONJUGADA DE INICIO O DE UNA MEZCLA DE ISOMEROS, UNA PRIMERA MONO-OLEFINA Y UNA SEGUNDA MONO-OLEFINA CON UN CATALIZADOR DE METATESIS BAJO CONDICIONES DE REACCION SELECCIONADAS PARA PRODUCIR UN PRODUCTO CON UN CONTENIDO DE ISOMEROS TRANS-GEOMETRICOS MAYOR DEL 80%. EN UNA CONFORMACION PREFERIDA 1,4 -HEXADIENO, ETENO Y PROPENO SE PONEN EN CONTACTO CON UN CATALIZADOR DE RE{SUB 2}O{SUB 7} Y SE CONVIERTEN EN UNA MEZCLA DE PRODUCTO DE REACCION CON ALREDEDOR DE UN 80% DE TRANS-1,4-HEXADIENO.
ES95906139T 1993-12-30 1994-12-30 Metodo para producir diolefinas trans no conjugadas. Expired - Lifetime ES2132621T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US17616693A 1993-12-30 1993-12-30

Publications (1)

Publication Number Publication Date
ES2132621T3 true ES2132621T3 (es) 1999-08-16

Family

ID=22643265

Family Applications (1)

Application Number Title Priority Date Filing Date
ES95906139T Expired - Lifetime ES2132621T3 (es) 1993-12-30 1994-12-30 Metodo para producir diolefinas trans no conjugadas.

Country Status (8)

Country Link
US (1) US5672803A (es)
EP (1) EP0737177B1 (es)
JP (1) JP3521912B2 (es)
AU (1) AU703293B2 (es)
CA (1) CA2180291C (es)
DE (1) DE69417443T2 (es)
ES (1) ES2132621T3 (es)
WO (1) WO1995018085A1 (es)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH10502691A (ja) * 1994-07-08 1998-03-10 ミネソタ マイニング アンド マニュファクチャリング カンパニー 過圧反応
DE19805716A1 (de) * 1998-02-12 1999-08-19 Basf Ag Verfahren zur Herstellung von Propen und gegebenenfalls 1-Buten
DE10046143A1 (de) * 2000-09-15 2002-05-29 Basf Ag Trägerfixierte Katalysatoren für die Olefin-Metathese
US7563936B2 (en) * 2006-10-27 2009-07-21 Honeywell International Inc Processes for geometric isomerization of halogenated olefins
US8530708B2 (en) * 2003-07-25 2013-09-10 Honeywell International Inc. Processes for selective dehydrohalogenation of halogenated alkanes
US7902410B2 (en) * 2005-11-03 2011-03-08 Honeywell International Inc. Process for the manufacture of fluorinated alkanes
KR101394583B1 (ko) * 2006-10-03 2014-05-12 멕시켐 아만코 홀딩 에스.에이. 데 씨.브이. 탄소수 3-6의 (하이드로)플루오로알켄의 생성을 위한 탈수소할로겐화 방법
US8013194B2 (en) 2008-03-14 2011-09-06 Honeywell International Inc. Process for the manufacture of fluorinated olefins
GB0706978D0 (en) 2007-04-11 2007-05-16 Ineos Fluor Holdings Ltd Process
US8710282B2 (en) 2008-03-14 2014-04-29 Honeywell International Inc. Integrated process for the manufacture of fluorinated olefins
GB201615209D0 (en) 2016-09-07 2016-10-19 Mexichem Fluor Sa De Cv Catalyst and process using the catalyst
GB201615197D0 (en) 2016-09-07 2016-10-19 Mexichem Fluor Sa De Cv Catalyst and process using the catalyst

Family Cites Families (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1054864A (es) * 1964-09-08 1900-01-01
US3405194A (en) * 1964-10-09 1968-10-08 Toray Industries Process for preparing hexadienes from conjugated diolefinic hydrocarbons and alpha-monoolefins
US3676520A (en) * 1964-12-31 1972-07-11 Phillips Petroleum Co Conversion of olefins
US3398209A (en) * 1965-07-06 1968-08-20 Goodrich Co B F Preparation of trans-1, 4-dienes
GB1103976A (en) * 1966-02-07 1968-02-21 British Petroleum Co Disproportionation process
US3502738A (en) * 1966-10-27 1970-03-24 Du Pont Preparation of 1,4-hexadiene from ethylene and butadiene with selected hydrocarbon-rhodium catalysts
US3424811A (en) * 1967-02-27 1969-01-28 Shell Oil Co Olefin production
NL137568C (es) * 1967-04-05
US3539652A (en) * 1968-10-31 1970-11-10 Goodrich Co B F Preparation of cis-1,4-dienes
US3641174A (en) * 1969-03-07 1972-02-08 Sun Oil Co Diolefin disproportionation reactions
US3565821A (en) * 1969-04-01 1971-02-23 Du Pont Process for activating phodium catalysts
US3565967A (en) * 1969-06-09 1971-02-23 Du Pont Process for manufacturing 1,4-dienes of high trans/cis ratio
DE2104626C2 (de) * 1970-02-09 1982-07-29 Mitsubishi Chemical Industries, Ltd., Tokyo Verfahren zur Herstellung eines Additionsproduktes eines konjugierten Diens und einer Verbindung mit endständiger Venylgruppe
US3907923A (en) * 1970-06-25 1975-09-23 Atlantic Richfield Co Oligomerization process
US3920763A (en) * 1970-07-09 1975-11-18 Atlantic Richfield Co Palladium catalyzed codimerization process
US3855338A (en) * 1973-10-24 1974-12-17 Hoffmann La Roche Preparation of 6-methyl-1,5-heptadiene
US3927137A (en) * 1974-03-18 1975-12-16 Goodyear Tire & Rubber Method of preparing nonconjugated diolefins
US4025570A (en) * 1976-01-09 1977-05-24 E. I. Du Pont De Nemours And Company Preparation of 1,4-dienes of high trans-isomer content
US4412089A (en) * 1981-08-24 1983-10-25 Shell Oil Company Process for the preparation of dienes and/or trienes
FR2606669B1 (fr) * 1986-11-18 1989-02-17 Inst Francais Du Petrole Procede de preparation d'un catalyseur renfermant du rhenium, catalyseur obtenu et utilisation de ce catalyseur pour la production d'olefines par metathese
GB8724628D0 (en) * 1987-10-21 1987-11-25 Bp Chem Int Ltd Chemical process
US5113033A (en) * 1990-01-12 1992-05-12 Exxon Chemical Patents Inc. Ruthenium salt and aluminum halide catalyst system for codimerization of alpha monoolefins and conjugated diolefins

Also Published As

Publication number Publication date
WO1995018085A1 (en) 1995-07-06
CA2180291C (en) 2006-01-17
JPH09508356A (ja) 1997-08-26
EP0737177A1 (en) 1996-10-16
CA2180291A1 (en) 1995-07-06
AU703293B2 (en) 1999-03-25
US5672803A (en) 1997-09-30
DE69417443T2 (de) 1999-11-18
JP3521912B2 (ja) 2004-04-26
DE69417443D1 (de) 1999-04-29
EP0737177B1 (en) 1999-03-24
AU1446995A (en) 1995-07-17

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