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. 2003 Oct 31;68(22):8669-82.
doi: 10.1021/jo030157k.

Catalytic intermolecular ortho-arylation of phenols

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Catalytic intermolecular ortho-arylation of phenols

Robin B Bedford et al. J Org Chem. .

Abstract

The use of rhodium catalysts such as [RhCl(PPh3)3] or [[RhCl(COD)]2] with PiPr2(OAr) or P(NMe2)3 co-catalysts allows the ortho-selective intermolecular arylation of phenols. The reaction proceeds via orthometalation of P-OAr groups and then transesterification liberates the product phenol. When 2-substituted phenols are used as substrates, [RhCl(PPh3)3]/iPr2(OAr) mixtures are typically the catalysts of choice, whereas for substrates without 2-substitution [[RhCl(COD)]2]/P(NMe2)3 mixtures tend to give better results.

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