Facile synthesis of alkyl- and arylboronate esters enabled by a carbon nanotube supported copper catalyst

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Date

2022-11-15T00:00:00

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Publisher

Royal Society of Chemistry

Abstract

An efficient synthesis of alkylboronate esters via alkyl halide borylation catalysed by copper nanoparticles stabilised on nitrogen-doped carbon nanotubes (N-CNT) is reported. This nanocatalyst provides practical access to alkylboronate esters at room temperature in 1 h, with good functional group tolerance. The procedure is also applicable to the borylation of benzyl chlorides and bromides. Radical clock experiments suggest that the reaction involves a radical pathway. The catalyst can be recycled up to ten runs without appreciable loss in the activity. In addition, we demonstrated the use of this supported copper catalyst for the anti-Markovnikov-selective hydroboration of vinylarenes and borylation of aryl halides with B2pin2, providing alkyl- and arylboronate esters, respectively, in good to excellent yields. � 2023 The Royal Society of Chemistry.

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Keywords

Carbon nanotubes, Catalyst supports, Chlorine compounds, Copper, Doping (additives), Esters, Metal halides, Synthesis (chemical), A-carbon, Alkylhalides, Arylboronates, Borylation, Copper catalyst, Copper nanoparticles, Efficient synthesis, Facile synthesis, Nano-catalyst, Nitrogen doped carbon nanotubes, Nanocatalysts

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