FR2939331B1 - Composition catalytique et procede de metathese de corps gras insature - Google Patents

Composition catalytique et procede de metathese de corps gras insature

Info

Publication number
FR2939331B1
FR2939331B1 FR0806935A FR0806935A FR2939331B1 FR 2939331 B1 FR2939331 B1 FR 2939331B1 FR 0806935 A FR0806935 A FR 0806935A FR 0806935 A FR0806935 A FR 0806935A FR 2939331 B1 FR2939331 B1 FR 2939331B1
Authority
FR
France
Prior art keywords
metathesis
catalytic composition
unsaturated body
unsaturated
catalytic
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.)
Active
Application number
FR0806935A
Other languages
English (en)
Other versions
FR2939331A1 (fr
Inventor
Cecilia Citadelle
Mikael Berthod
Severine Guibet
Bourbigou Helene Olivier
Christophe Vallee
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.)
IFP Energies nouvelles
Original Assignee
IFP Energies nouvelles
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 IFP Energies nouvelles filed Critical IFP Energies nouvelles
Priority to FR0806935A priority Critical patent/FR2939331B1/fr
Priority to PCT/FR2009/001359 priority patent/WO2010066959A1/fr
Publication of FR2939331A1 publication Critical patent/FR2939331A1/fr
Application granted granted Critical
Publication of FR2939331B1 publication Critical patent/FR2939331B1/fr
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • 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
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22—Organic complexes
    • B01J31/2265—Carbenes or carbynes, i.e.(image)
    • B01J31/2269—Heterocyclic carbenes
    • B01J31/2273—Heterocyclic carbenes with only nitrogen as heteroatomic ring members, e.g. 1,3-diarylimidazoline-2-ylidenes
    • 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
    • B01J31/0277—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature
    • B01J31/0278—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing nitrogen as cationic centre
    • B01J31/0281—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing nitrogen as cationic centre the nitrogen being a ring member
    • B01J31/0284—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing nitrogen as cationic centre the nitrogen being a ring member of an aromatic ring, e.g. pyridinium
    • 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
    • B01J31/0277—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature
    • B01J31/0287—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing atoms other than nitrogen as cationic centre
    • B01J31/0288—Phosphorus
    • 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
    • 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
    • B01J2231/54—Metathesis reactions, e.g. olefin metathesis
    • B01J2231/543—Metathesis reactions, e.g. olefin metathesis alkene metathesis
    • 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
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82—Metals of the platinum group
    • B01J2531/821—Ruthenium
    • 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
    • C07C2531/22—Organic complexes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
FR0806935A 2008-12-10 2008-12-10 Composition catalytique et procede de metathese de corps gras insature Active FR2939331B1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
FR0806935A FR2939331B1 (fr) 2008-12-10 2008-12-10 Composition catalytique et procede de metathese de corps gras insature
PCT/FR2009/001359 WO2010066959A1 (fr) 2008-12-10 2009-11-30 Composition catalytique et procede de metathese de corps gras insature.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR0806935A FR2939331B1 (fr) 2008-12-10 2008-12-10 Composition catalytique et procede de metathese de corps gras insature

Publications (2)

Publication Number Publication Date
FR2939331A1 FR2939331A1 (fr) 2010-06-11
FR2939331B1 true FR2939331B1 (fr) 2012-08-10

Family

ID=40874636

Family Applications (1)

Application Number Title Priority Date Filing Date
FR0806935A Active FR2939331B1 (fr) 2008-12-10 2008-12-10 Composition catalytique et procede de metathese de corps gras insature

Country Status (2)

Country Link
FR (1) FR2939331B1 (fr)
WO (1) WO2010066959A1 (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109304165B (zh) * 2017-07-28 2021-10-01 中国石油化工股份有限公司 甘油合成丙烯酸催化剂

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1253156A3 (fr) 1992-04-03 2004-01-07 California Institute Of Technology Composé ruthénium et osmium métal-carbène avec haute activité de la méthathèse d'oléfines, et leur préparation et utilisation
EP0921129A1 (fr) 1997-12-03 1999-06-09 Studiengesellschaft Kohle mbH Complexes de ruthénium et d'osmium cationiques hautement actifs pour les réactions de métathèse des oléfines
DE19815275B4 (de) 1998-04-06 2009-06-25 Evonik Degussa Gmbh Alkylidenkomplexe des Rutheniums mit N-heterozyklischen Carbenliganden und deren Verwendung als hochaktive, selektive Katalysatoren für die Olefin-Metathese
KR100823365B1 (ko) 1999-05-24 2008-04-17 캘리포니아 인스티튜트 오브 테크놀로지 이미다졸리딘계 금속 카르벤 복분해 촉매
WO2002014376A2 (fr) 2000-08-10 2002-02-21 Trustees Of Boston College Catalyseurs de metathese recyclables
US7205424B2 (en) 2003-06-19 2007-04-17 University Of New Orleans Research And Technology Foundation, Inc. Preparation of ruthenium-based olefin metathesis catalysts
US7176336B2 (en) 2003-10-09 2007-02-13 Dow Global Technologies Inc. Process for the synthesis of unsaturated alcohols
FR2878246B1 (fr) * 2004-11-23 2007-03-30 Inst Francais Du Petrole Procede de co-production d'olefines et d'esters par ethenolyse de corps gras insatures dans des liquides ioniques non-aqueux
GB0514612D0 (en) 2005-07-15 2005-08-24 Sasol Technology Uk Ltd The use of a phosphorus containing ligand and a cyclic organic ligand in a metathesis catalyst
ES2349861T3 (es) 2005-11-09 2011-01-12 Boehringer Ingelheim International Gmbh Preparación de catalizadores.
US8008224B2 (en) 2005-12-16 2011-08-30 Materia, Inc. Organometallic ruthenium complexes and related methods for the preparation of tetra-substituted and other hindered olefins
FR2896500B1 (fr) * 2006-01-24 2010-08-13 Inst Francais Du Petrole Procede de co-production d'olefines et de diesters ou de diacides par homometathese de corps gras insatures dans des liquides ioniques non-aqueux.
FR2896498B1 (fr) * 2006-01-24 2008-08-29 Inst Francais Du Petrole Procede de co-production d'olefines et de diesters ou de diacides a partir de corps gras insatures.
WO2008010961A2 (fr) 2006-07-13 2008-01-24 Elevance Renewable Sciences, Inc. Synthèse d'alcènes à double liaison terminale à partir d'alcènes à double liaison interne et d'éthylène via la métathèse d'oléfines

Also Published As

Publication number Publication date
WO2010066959A1 (fr) 2010-06-17
FR2939331A1 (fr) 2010-06-11

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