1146593-95-4Relevant articles and documents
CATALYST FOR CROSS-COUPLING REACTION, AND PROCESS FOR PRODUCTION OF AROMATIC COMPOUND USING THE SAME
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Page/Page column 21, (2011/07/06)
The present invention provides a process for efficiently producing an alkylated aromatic compound in good yield, by a cross-coupling reaction between an alkyl halide and an aromatic magnesium reagent. A process for producing an aromatic compound represented by Formula (1): [in-line-formulae]R—Ar′??(1)[/in-line-formulae]wherein R is a hydrocarbon group, and Ar′ is an aryl group;the process comprising:reacting a compound represented by Formula (2): [in-line-formulae]R—X??(2)[/in-line-formulae]wherein X is a halogen atom, and R is as defined above, with a magnesium reagent represented by Formula (3): [in-line-formulae]Ar′—MgY??(3)[/in-line-formulae]wherein Y is a halogen atom, and Ar′ is as defined above, in the presence of a catalyst for cross-coupling reactions comprising an iron compound and a bisphosphine compound represented by Formula (4): wherein Q is a divalent group derived from an aromatic ring by removing two hydrogen (H) atoms on adjacent carbon atoms; and each Ar is independently an aryl group.
Iron-catalysed fluoroaromatic coupling reactions under catalytic modulation with 1,2-bis(diphenylphosphino)benzene
Hatakeyama, Takuji,Kondo, Yoshiyuki,Fujiwara, Yu-Ichi,Takaya, Hikaru,Ito, Shingo,Nakamura, Eiichi,Nakamura, Masaharu
supporting information; experimental part, p. 1216 - 1218 (2009/07/10)
A catalytic amount of 1,2-bis(diphenylphosphino)benzene (DPPBz) achieves selective cleavage of sp3-carbon-halogen bond in the iron-catalysed cross-coupling between polyfluorinated arylzinc reagents and alkyl halides, which was unachievable with
