Issue 5, 2024

A convenient synthetic approach to highly hindered 3,3′-bis(2,4,6-tri-tert-butylphenyl)-BINOL-derived phosphoric acids

Abstract

Considering the success of BINOL phosphoric acids and a serious lack of preparation methods for hindered chiral phosphoric acid catalysts, herein we present an efficient approach to highly hindered (S) and (R)-3,3′-bis(2,4,6-tri-tert-butylphenyl)-BINOL-derived phosphoric acids with high enantioselectivity. Direct arylations of the C–F bonds in optically pure 3,3′-difluoro-BINOL derivatives with (2,4,6-tri-tert-butylphenyl)magnesium bromide were explored as the key transformation. Optical resolution chromatography was avoided and both enantiomers were successfully prepared on a ten-gram-scale via our method.

Graphical abstract: A convenient synthetic approach to highly hindered 3,3′-bis(2,4,6-tri-tert-butylphenyl)-BINOL-derived phosphoric acids

Supplementary files

Article information

Article type
Communication
Submitted
16 Nov 2023
Accepted
03 Jan 2024
First published
04 Jan 2024

New J. Chem., 2024,48, 1898-1901

A convenient synthetic approach to highly hindered 3,3′-bis(2,4,6-tri-tert-butylphenyl)-BINOL-derived phosphoric acids

Z. Wang and G. Li, New J. Chem., 2024, 48, 1898 DOI: 10.1039/D3NJ05280J

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