An Effective Catalytic Hydroboration of Alkynes in Supercritical CO2 under Repetitive Batch Mode

A facile method for the synthesis of unsaturated organoboron compounds by hydroboration of terminal and internal alkynes in supercritical (sc) CO2 has been presented for the first time. The reactions performed in scCO2 in the presence of Ru catalysts (selectivity, productivity) are compared with tho...

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Published inChemCatChem Vol. 10; no. 3; pp. 531 - 539
Main Authors Szyling, Jakub, Franczyk, Adrian, Stefanowska, Kinga, Klarek, Mateusz, Maciejewski, Hieronim, Walkowiak, Jędrzej
Format Journal Article
LanguageEnglish
Published Weinheim Wiley Subscription Services, Inc 07.02.2018
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Summary:A facile method for the synthesis of unsaturated organoboron compounds by hydroboration of terminal and internal alkynes in supercritical (sc) CO2 has been presented for the first time. The reactions performed in scCO2 in the presence of Ru catalysts (selectivity, productivity) are compared with those in a traditionally used solvent or without it. Moreover, the catalytic systems based on the application of scCO2 have been successfully tested for the processes under repetitive batch conditions. This strategy permitted us to obtain boryl‐substituted olefins with high yields and selectivities up to the 16th catalytic cycle if using Ru(CO)Cl(H)(PPh3)3 as a catalyst. The process applied the self‐dosing catalyst, which is gradually released to the reaction mixture under supercritical conditions in the individual batch. Such an approach has a positive impact on process sustainability and economy. Batch by batch: A facile method for the synthesis of unsaturated organoboron compounds by hydroboration of terminal and internal alkynes in supercritical (sc) CO2 is presented. The scCO2 catalytic systems have been successfully tested for the processes under repetitive batch conditions. This strategy permitted boryl‐substituted olefins to be obtained with high yields and selectivities up to the 16th catalytic cycle if using Ru(CO)Cl(H)(PPh3)3 as a catalyst.
ISSN:1867-3880
1867-3899
DOI:10.1002/cctc.201701318