To provide a method by which an objective biaryl can be obtained in good yield without forming harmful by-products, especially the method suitable for the mass-production of the biaryl.
An aryl halide represented by formula (I) (wherein, Ar1 is a monovalent aryl group; X is a halogen atom) is reacted with an alcohol compound represented by formula (II) (wherein, Ar2 is a monovalent aryl group; R1 and R2 are each independently hydrogen atom, an alkyl group or an aryl group same as the Ar2; R1 and R2 may bond to each other to form a divalent group; with the proviso that the case of forming an indenylidene group from the R1 in combination with the R2 is omitted) to provide the objective aromatic compound represented by formula (III) (wherein, Ar1 and Ar2 have the same meanings as the above).
SATO TETSUYA
NOMURA MASAKATSU
SATO TETSUYA
NOMURA MASAKATSU
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