Regioselective Boracarboxylation of α-Substituted Vinyl Arenes

13 April 2022, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

An experimental study of the effect of CO2 pressure on the copper(I)-catalyzed boracarboxylation of α-substituted vinyl arenes is reported. Preliminary experiments using ICyCuCl catalyst (ICy = 1,3-bis(cyclohexyl)imidazol-2-ylidine) showed that boracarboxylation of tert-butylstyrene can be achieved in 30 minutes at modest CO2 pressure (3-6 atm) as opposed to 24-36 hours at atmospheric pressure. Due to increased substrate sterics that allowed catalytic reduction of CO2 to compete kinetically, boracarboxylation of a-methyl styrene, even at modest CO2 pressures, gave poor yields. Low CO2 pressure and SIMesCuCl catalyst (SIMes = 1,3-bis(2,4,6-trimethylphenyl)imidazol-4,5-dihydro-2-ylidine) provided moderate to good yields of an electronically and sterically diverse group of quaternary carboxylic acid products featuring a -boronic ester functional group.

Keywords

copper catalysis
alkene difunctionalization
carbon dioxide
boronic ester

Supplementary materials

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Description
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Supporting Information
Description
1H, 13C, 11B, and 19F NMR spectra for new boracarboxylated compounds.
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