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WO2002013964A3 - Zur herstellung von nutrilen geeigneter katalysator - Google Patents

Zur herstellung von nutrilen geeigneter katalysator Download PDF

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Publication number
WO2002013964A3
WO2002013964A3 PCT/EP2001/008522 EP0108522W WO0213964A3 WO 2002013964 A3 WO2002013964 A3 WO 2002013964A3 EP 0108522 W EP0108522 W EP 0108522W WO 0213964 A3 WO0213964 A3 WO 0213964A3
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WO
WIPO (PCT)
Prior art keywords
independently represent
different
same
suitable catalyst
formula
Prior art date
Application number
PCT/EP2001/008522
Other languages
English (en)
French (fr)
Other versions
WO2002013964A2 (de
Inventor
Michael Bartsch
Dagmar Pascale Kunsmann-Keitel
Robert Baumann
Gerd Haderlein
Wolfgang Siegel
Original Assignee
Basf Ag
Michael Bartsch
Dagmar Pascale Kunsmann-Keitel
Robert Baumann
Gerd Haderlein
Wolfgang Siegel
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 Basf Ag, Michael Bartsch, Dagmar Pascale Kunsmann-Keitel, Robert Baumann, Gerd Haderlein, Wolfgang Siegel filed Critical Basf Ag
Priority to AU2001282012A priority Critical patent/AU2001282012A1/en
Publication of WO2002013964A2 publication Critical patent/WO2002013964A2/de
Publication of WO2002013964A3 publication Critical patent/WO2002013964A3/de

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F15/00Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
    • C07F15/04Nickel compounds
    • C07F15/045Nickel compounds without a metal-carbon linkage
    • 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
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/18Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
    • B01J31/1845Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing phosphorus
    • B01J31/185Phosphites ((RO)3P), their isomeric phosphonates (R(RO)2P=O) and RO-substitution derivatives thereof
    • 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
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/18Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
    • B01J31/1845Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing phosphorus
    • B01J31/1865Phosphonites (RP(OR)2), their isomeric phosphinates (R2(RO)P=O) and RO-substitution derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/06Phosphorus compounds without P—C bonds
    • C07F9/08Esters of oxyacids of phosphorus
    • C07F9/141Esters of phosphorous acids
    • C07F9/145Esters of phosphorous acids with hydroxyaryl compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/28Phosphorus compounds with one or more P—C bonds
    • C07F9/46Phosphinous acids [R2POH], [R2P(= O)H]: Thiophosphinous acids including[R2PSH]; [R2P(=S)H]; Aminophosphines [R2PNH2]; Derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/28Phosphorus compounds with one or more P—C bonds
    • C07F9/48Phosphonous acids [RP(OH)2] including [RHP(=O)(OH)]; Thiophosphonous acids including [RP(SH)2], [RHP(=S)(SH)]; Derivatives thereof
    • C07F9/4866Phosphonous acids [RP(OH)2] including [RHP(=O)(OH)]; Thiophosphonous acids including [RP(SH)2], [RHP(=S)(SH)]; Derivatives thereof the ester moiety containing a substituent or structure which is considered as characteristic
    • C07F9/4875Esters with hydroxy aryl compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6564Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
    • C07F9/6571Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms
    • C07F9/6574Esters of oxyacids of phosphorus
    • C07F9/65746Esters of oxyacids of phosphorus the molecule containing more than one cyclic phosphorus atom
    • 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
    • B01J2231/30Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
    • B01J2231/32Addition reactions to C=C or C-C triple bonds
    • B01J2231/323Hydrometalation, e.g. bor-, alumin-, silyl-, zirconation or analoguous reactions like carbometalation, hydrocarbation
    • 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80Complexes comprising metals of Group VIII as the central metal
    • B01J2531/84Metals of the iron group
    • B01J2531/847Nickel
    • 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
    • B01J31/26Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24
    • B01J31/28Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24 of the platinum group metals, iron group metals or copper

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Inorganic 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)
  • Catalysts (AREA)

Abstract

Katalysator, enthaltend einen Nickel (0) komplex mit einem Liganden der Formel (I): Y1 - E1 - X - E2 - Y2, worin X für Arylen oder Heteroarylen steht, E1, E2 unabhängig voneinander für O oder NZ5 steht, Y1, Y2 gleich oder unterschliedlich sein können und unabhängig voneinander für einen Rest der Formeln (II.1): -P(-E?3-R1)(-E4-R2¿) oder (II.2) stehen, worin E?3, E4, E5, E6¿ gleich oder verschieden sein können und unabhängig voneinander eine chemische Bindung sein können oder unabhängig voneinander für O oder NZ11 steht, R1, R2 gleich oder verschieden sein können und unabhängig voneinander eine Cycloalkyl-, Aryl-, Heterocycloalkyl- oder Heteroarylgruppe, R3 zusammen mit dem Teil des Systems -E5-P-E6-, an den es gebunden ist, für einen 5-, 6-, 7- oder 8-gliedrigen Heterocyclus steht.
PCT/EP2001/008522 2000-08-02 2001-07-24 Zur herstellung von nutrilen geeigneter katalysator WO2002013964A2 (de)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU2001282012A AU2001282012A1 (en) 2000-08-02 2001-07-24 Suitable catalyst for producing nitriles

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10038037.9 2000-08-02
DE2000138037 DE10038037A1 (de) 2000-08-02 2000-08-02 Zur Herstellung von Nitrilen geeigneter Katalysator und Verfahren zur Herstellung von Nitrilen

Publications (2)

Publication Number Publication Date
WO2002013964A2 WO2002013964A2 (de) 2002-02-21
WO2002013964A3 true WO2002013964A3 (de) 2002-07-18

Family

ID=7651302

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2001/008522 WO2002013964A2 (de) 2000-08-02 2001-07-24 Zur herstellung von nutrilen geeigneter katalysator

Country Status (4)

Country Link
AR (1) AR030084A1 (de)
AU (1) AU2001282012A1 (de)
DE (1) DE10038037A1 (de)
WO (1) WO2002013964A2 (de)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8906334B2 (en) 2007-05-14 2014-12-09 Invista North America S.A R.L. High efficiency reactor and process

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10136488A1 (de) 2001-07-27 2003-02-06 Basf Ag Ni(O) enthaltendes Katalysatorsystem
FR2842196B1 (fr) * 2002-07-15 2006-01-13 Rhodia Polyamide Intermediates Procede de fabrication de composes nitriles a partir de composes a insaturation ethylenique
FR2850966B1 (fr) 2003-02-10 2005-03-18 Rhodia Polyamide Intermediates Procede de fabrication de composes dinitriles
US7786349B2 (en) 2003-04-09 2010-08-31 Bayer Bioscience N.V. Methods and means for increasing the tolerance of plants to stress conditions
FR2854891B1 (fr) 2003-05-12 2006-07-07 Rhodia Polyamide Intermediates Procede de preparation de dinitriles
DE102004004718A1 (de) 2004-01-29 2005-08-18 Basf Ag Verfahren zur Hydrocyanierung
US7973174B2 (en) 2005-10-18 2011-07-05 Invista North America S.A.R.L. Process of making 3-aminopentanenitrile
WO2007109005A2 (en) 2006-03-17 2007-09-27 Invista Technologies S.A R.L. Method for the purification of triorganophosphites by treatment with a basic additive
AU2007251879B2 (en) 2006-05-12 2013-01-10 Bayer Cropscience Nv Novel stress-related microrna molecules and uses thereof
US7919646B2 (en) 2006-07-14 2011-04-05 Invista North America S.A R.L. Hydrocyanation of 2-pentenenitrile
US7880028B2 (en) 2006-07-14 2011-02-01 Invista North America S.A R.L. Process for making 3-pentenenitrile by hydrocyanation of butadiene
CN101952004B (zh) 2007-06-13 2015-08-12 因温斯特技术公司 改善己二腈质量的方法
EP2229354B1 (de) 2008-01-15 2013-03-20 Invista Technologies S.à.r.l. Verfahren zur herstellung und verfeinerung von 3-pentennitril und zur verfeinerung von 2-methyl-3-butennitril
EP2229353B1 (de) 2008-01-15 2018-01-03 INVISTA Textiles (U.K.) Limited Hydrocyanierung von pentennitrilen
FR2926816B1 (fr) 2008-01-25 2010-05-14 Rhodia Operations Procede de fabrication de composes comprenant des fonctions nitriles
FR2932477B1 (fr) 2008-06-17 2013-01-18 Rhodia Operations Procede de fabrication de composes nitriles a partir de composes a insaturation ethylenique
JP5619753B2 (ja) 2008-10-14 2014-11-05 インヴィスタテクノロジーズ エスアエルエル 2−第二級−アルキル−4,5−ジ−(直鎖−アルキル)フェノール類を製造する方法
FR2937321B1 (fr) 2008-10-21 2010-10-22 Rhodia Operations Procede de fabrication de composes comprenant des fonctions nitriles
FR2941455B1 (fr) 2009-01-29 2011-02-11 Rhodia Operations Procede de fabrication de composes comprenant des fonctions nitriles
JP5615920B2 (ja) 2009-08-07 2014-10-29 インヴィスタ テクノロジーズ エスアエルエル ジエステルを形成するための水素化およびエステル化
JP5705986B2 (ja) 2010-09-07 2015-04-22 インヴィスタ テクノロジーズ エスアエルエル ニッケル金属およびニッケル錯体を調製するためのニッケル組成物

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0214622A2 (de) * 1985-09-05 1987-03-18 Union Carbide Corporation Durch Übergangsmetallkomplexe katalysierte Herstellungsverfahren
EP0518241A2 (de) * 1991-06-11 1992-12-16 Mitsubishi Chemical Corporation Hydroformylierungsverfahren und darin verwendete Bisphosphitverbindung
WO1996022968A1 (en) * 1995-01-27 1996-08-01 E.I. Du Pont De Nemours And Company Hydrocyanation of diolefins and isomerization of nonconjugated 2-alkyl-3-monoalkenenitriles
WO1999006357A1 (en) * 1997-07-29 1999-02-11 E.I. Du Pont De Nemours And Company Hydrocyanation of diolefins and isomerization of nonconjugated 2-alykl-3-monoalkenenitriles

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0214622A2 (de) * 1985-09-05 1987-03-18 Union Carbide Corporation Durch Übergangsmetallkomplexe katalysierte Herstellungsverfahren
EP0518241A2 (de) * 1991-06-11 1992-12-16 Mitsubishi Chemical Corporation Hydroformylierungsverfahren und darin verwendete Bisphosphitverbindung
WO1996022968A1 (en) * 1995-01-27 1996-08-01 E.I. Du Pont De Nemours And Company Hydrocyanation of diolefins and isomerization of nonconjugated 2-alkyl-3-monoalkenenitriles
WO1999006357A1 (en) * 1997-07-29 1999-02-11 E.I. Du Pont De Nemours And Company Hydrocyanation of diolefins and isomerization of nonconjugated 2-alykl-3-monoalkenenitriles

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
BAKER M J ET AL: "Chiral aryl diphosphites: a new class of ligands for hydrocyanation catalysis", CHEMICAL COMMUNICATIONS, ROYAL SOCIETY OF CHEMISTRY, GB, no. 18, 1991, pages 1292 - 1293, XP002180130, ISSN: 1359-7345 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8906334B2 (en) 2007-05-14 2014-12-09 Invista North America S.A R.L. High efficiency reactor and process

Also Published As

Publication number Publication date
AR030084A1 (es) 2003-08-13
WO2002013964A2 (de) 2002-02-21
DE10038037A1 (de) 2002-04-18
AU2001282012A1 (en) 2002-02-25

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