This work demonstrates efficient C-H alkynylation of indoles in biobased Cyrene, indicating a sustainable method with mechanistic insights from DFT studies.
Transition metal-catalyzed C-H activation reactions are desirable as they fulfill several principles of green chemistry. However, these reactions often use toxic and volatile organic solvents, significantly hampering the sustainability of the C-H activation strategy. In this work, we demonstrate the use of biobased Cyrene as the solvent for the rhodium(III)-catalyzed C-H alkynylation of indoles. The reaction was performed at room temperature with a shorter reaction time. Detailed mechanistic studies were conducted to understand the reaction mechanism. Supported by DFT calculations and experimental studies, a plausible catalytic cycle was proposed, involving α-halogen elimination and silyl transfer as the key steps in the C-H alkynylation. The rhodium(III)-catalyzed C-H alkynylation in Cyrene media has been studied for the robustness of the reaction conditions by evaluating its reaction-condition-based sensitivity. Furthermore, the green chemistry metrics calculations suggested that the developed protocol is highly efficient and eco-friendly.
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Maayuri et al. (2025) studied this question.
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