WO2002026665A3 - Verfahren zur herstellung von arylverbindungen - Google Patents

Verfahren zur herstellung von arylverbindungen Download PDF

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Publication number
WO2002026665A3
WO2002026665A3 PCT/EP2001/010558 EP0110558W WO0226665A3 WO 2002026665 A3 WO2002026665 A3 WO 2002026665A3 EP 0110558 W EP0110558 W EP 0110558W WO 0226665 A3 WO0226665 A3 WO 0226665A3
Authority
WO
WIPO (PCT)
Prior art keywords
aryl compounds
grignard reagent
substituted aryl
producing aryl
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.)
Ceased
Application number
PCT/EP2001/010558
Other languages
English (en)
French (fr)
Other versions
WO2002026665A2 (de
Inventor
Markus Eckert
Guido Giffels
Hans-Christian Militzer
Thomas Prinz
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.)
Bayer AG
Original Assignee
Bayer AG
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
Priority claimed from DE2000147484 external-priority patent/DE10047484A1/de
Priority claimed from DE2001121105 external-priority patent/DE10121105A1/de
Application filed by Bayer AG filed Critical Bayer AG
Priority to AU2002218171A priority Critical patent/AU2002218171A1/en
Priority to EP01985697A priority patent/EP1324964A2/de
Publication of WO2002026665A2 publication Critical patent/WO2002026665A2/de
Publication of WO2002026665A3 publication Critical patent/WO2002026665A3/de
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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
    • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/02—Impregnation, coating or precipitation
    • B01J37/0201—Impregnation
    • B01J37/0203—Impregnation the impregnation liquid containing organic 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
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/74—Iron group metals
    • B01J23/755—Nickel
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B37/00—Reactions without formation or introduction of functional groups containing hetero atoms, involving either the formation of a carbon-to-carbon bond between two carbon atoms not directly linked already or the disconnection of two directly linked carbon atoms
    • C07B37/04—Substitution

Landscapes

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

Abstract

Arylverbindungen werden in vorteilhafter Weise durch Kreuzkupplungsreaktion einer substituierten Arylverbindung mit einem Grignard-Reagenz unter Nickelkatalyse hergestellt, wenn man substituierte Arylverbindungen und einen neuartigen Nickelkatalysator vorlegt und bei Reaktionstemperatur das Grignard-Reagenz zudosiert.
PCT/EP2001/010558 2000-09-26 2001-09-13 Verfahren zur herstellung von arylverbindungen Ceased WO2002026665A2 (de)

Priority Applications (2)

Application Number Priority Date Filing Date Title
AU2002218171A AU2002218171A1 (en) 2000-09-26 2001-09-13 Method for producing aryl compounds
EP01985697A EP1324964A2 (de) 2000-09-26 2001-09-13 Verfahren zur herstellung von arylverbindungen

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
DE2000147484 DE10047484A1 (de) 2000-09-26 2000-09-26 Verfahren zur Herstellung von Arylverbindungen
DE10047484.5 2000-09-26
DE2001121105 DE10121105A1 (de) 2001-04-27 2001-04-27 Verfahren zur Herstellung von Arylverbindungen
DE10121105.8 2001-04-27

Publications (2)

Publication Number Publication Date
WO2002026665A2 WO2002026665A2 (de) 2002-04-04
WO2002026665A3 true WO2002026665A3 (de) 2002-11-07

Family

ID=26007157

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2001/010558 Ceased WO2002026665A2 (de) 2000-09-26 2001-09-13 Verfahren zur herstellung von arylverbindungen

Country Status (5)

Country Link
US (1) US20020077250A1 (de)
EP (1) EP1324964A2 (de)
CN (1) CN1289190C (de)
AU (1) AU2002218171A1 (de)
WO (1) WO2002026665A2 (de)

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* Cited by examiner, † Cited by third party
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JP2009507032A (ja) 2005-09-02 2009-02-19 アボット・ラボラトリーズ 新規なイミダゾ系複素環
CN103877995B (zh) * 2014-03-31 2016-02-17 陕西师范大学 蒙脱土负载纳米Pd/Cu催化剂及其原位一锅法制备和应用
CN106146454B (zh) * 2016-07-01 2018-08-24 陕西师范大学 Negishi偶联制备多氟联芳烃类化合物的方法
CN106187656B (zh) * 2016-07-01 2018-10-23 陕西师范大学 镁辅助镍催化多氟芳烃单芳基化的方法
CN106243018B (zh) * 2016-07-26 2018-09-21 陕西师范大学 一种多氟苯基吡啶类化合物的合成方法
US9687837B1 (en) 2016-08-31 2017-06-27 Eastman Chemical Company Stable hydroformylation catalyst for preparation of high N/Iso ratio aldehyde product
US9975833B2 (en) 2016-08-31 2018-05-22 Eastman Chemical Company Efficient catalyst for the formation of polyaryl hydrocarbons suitable as precursors for polydentate organophosphorus catalyst ligands
CN107266282B (zh) * 2017-07-25 2020-06-30 利尔化学股份有限公司 一种1,4-二甲基萘的制备方法
CN109053359B (zh) * 2018-06-29 2021-09-07 万华化学集团股份有限公司 一种四烃基取代联苯的制备方法
CN112675850A (zh) * 2020-12-23 2021-04-20 江苏广域化学有限公司 镍催化剂、其制备方法及嘧啶类衍生物的合成方法

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0262389A1 (de) * 1986-08-30 1988-04-06 BASF Aktiengesellschaft Verfahren zur Herstellung von medizinischen Weissölen und medizinischen Paraffinen

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0262389A1 (de) * 1986-08-30 1988-04-06 BASF Aktiengesellschaft Verfahren zur Herstellung von medizinischen Weissölen und medizinischen Paraffinen

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
GANDIA L.M., MONTES M.: "Effect of Thermal Treatments on the Properties of Nickel and Cobalt Activated-Charcoal-Supported Catalysts", J. CATAL., vol. 145, 1994, pages 276 - 288, XP002194527 *
IKOMA Y ET AL.: "Non-ligated Nickel Chloride-Catalyzed Cross-Coupling of Aromatic Grignard Reagents with Aryl Halides", SYNTHESIS, 1990, pages 147 - 8, XP002194436 *
LIPSHUTZ B.H.: "Development of Nickel-on-Charcoal as a "dirt-Cheap" Heterogeneous Catalyst: A Personal Account", ADV. SYNTH. CATAL., vol. 343, no. 4, 8 June 2001 (2001-06-08), XP002194454 *
LIPSHUTZ ET AL-: "Kumada couplings catalyzed by nickel on charcoal (Ni/C)", INORG. CHIM. ACTA, vol. 296, 1999, pages 164 - 9, XP002194453 *
TAMAO K ET AL: "NICKEL-PHOSPHINE COMPLEX-CATALYZED GRIGNARD COUPLING. I. CROSS-COUPLING OF ALKYL, ARYL, AND ALKENYL GRIGNARD REAGENTS WITH ARYL AND ALKENYL HALIDES: GENERAL SCOPE AND LIMITATIONS", BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, JAPAN PUBLICATIONS TRADING CO. TOKYO, JP, vol. 49, no. 7, July 1976 (1976-07-01), pages 1958 - 1969, XP000996380, ISSN: 0009-2673 *

Also Published As

Publication number Publication date
US20020077250A1 (en) 2002-06-20
EP1324964A2 (de) 2003-07-09
AU2002218171A1 (en) 2002-04-08
CN1289190C (zh) 2006-12-13
CN1466487A (zh) 2004-01-07
WO2002026665A2 (de) 2002-04-04

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