Visible-light-induced and EDA complex-driven multicomponent reaction: a strategy for the synthesis of α-CF3-β-phosphorodithioate tertiary alcohols

Abstract

A green and efficient synthetic strategy has been developed for the construction of α-trifluoromethyl-β-phosphorodithioate tertiary alcohols from trifluoromethyl alkenes, O2, P4S10, and alcohols via a visible-light-promoted, electron donor–acceptor (EDA) complex-driven four-component reaction. This reaction proceeds at room temperature under photocatalyst-free, metal-free, and additive-free conditions. The reaction features simple operation, mild reaction conditions, and excellent compatibility with various functional groups. In addition, air (O2) serves as a sustainable oxygen source in this reaction, facilitating the modification of bioactive molecules. Detailed experimental studies and theoretical density functional theory (DFT) calculations suggest that the reaction likely proceeds via an EDA complex-mediated radical pathway.

Graphical abstract: Visible-light-induced and EDA complex-driven multicomponent reaction: a strategy for the synthesis of α-CF3-β-phosphorodithioate tertiary alcohols

Supplementary files

Article information

Article type
Paper
Submitted
18 Mar 2025
Accepted
22 Jul 2025
First published
23 Jul 2025

Green Chem., 2025, Advance Article

Visible-light-induced and EDA complex-driven multicomponent reaction: a strategy for the synthesis of α-CF3-β-phosphorodithioate tertiary alcohols

M. Wang, Z. Chen, F. Xue, Q. Tan, B. Wang, Y. Zhang, Y. Xia, S. Wu, W. Jin, X. Jiang and C. Liu, Green Chem., 2025, Advance Article , DOI: 10.1039/D5GC01349F

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