Year: 2024
Type: article
Abstract: The selective double hydroboration of CO 2 into bis(boryl)acetal (BBA) is a challenging yet appealing reduction process since BBA can be used as a versatile C 1 and C n sources for the synthesis of value-added products. In the present study, we demonstrate that simple borohydride compounds are efficient and selective catalysts for the synthesis of BBA when using 9-borabicyclo(3.3.1)nonane (9-BBN) as a reductant. The experimental and theoretical investigations show that while the borohydride species catalyzes the first reduction step of CO 2 into formoxyborane (2e – reduction intermediate), the observed 4e – reduction selectivity is mostly due to the ability of 9-BBN to reduce the formoxyborane into BBA without a catalyst. Notably, 0.2 mol % of LiH 2 BBN catalyzed the hydroboration of CO 2 with 9-BBN as a reductant into the corresponding BBA in 77% yield with TON and TOF of 385 and 196 h –1, respectively. The simplicity of borohydride contrasts with the more elaborate catalytic systems used so far for the 4e – reduction of CO 2 .
Source: The Journal of Organic Chemistry
Authors: Carlos Jarava-Barrera, Sarah Desmons, Dan Zhang, Laure Vendier, Qingli Xu, Nana Ma, Sébastien Bontemps
Language: English
Subfield: Process Chemistry and Technology
Field: Chemical Engineering
Domain: Physical Sciences
SDG: Climate action
Open Access status: green
Award: Inorganic Calvin Cycle
OpenAlex ID: W4401733413
