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Updated: Jul 23, 2025

Versatile CO2 Transformations into Complex Products: A One-pot Two-step Strategy
Published on: November 9, 2019
One-Step Electrocatalytic Approach Applied to the Synthesis of β-Propiolactones from CO2 and Dienes
Renate Schwiedernoch1, Xiaofeng Niu1, Haosheng Shu1
1Eco-Efficient Products and Processes Laboratory (E2P2L, IRL 3464 CNRS-Solvay), Solvay (China) Co., Ltd., 3966 Jindu Road, Xinzhuang Industrial Zone, Shanghai 201108, P. R. China.
Abstract:
β-Lactones are common substructures in a variety of natural products and drugs, and they serve as versatile synthetic intermediates in the production of valuable chemical derivatives. Traditional β-lactone synthesis relies on laborious multi-step synthetic methods that use toxic compounds, sophisticated catalysts, expensive, and/or reactive chemicals. Based on the in situ electrochemical formation of metal-based nanoclusters, this paper describes the development of a one-step, room temperature electrocatalytic method for the formation of stable β-lactone from CO2 and dienes. This one-step "electrosynthesis" method results in the formation of a new class of β-lactone with high selectivity (up to 100%) and activity (up to 80% yields with respect to the reacted diene) by regulating the applied potential and current density. This work paves the way for more sustainable and environmentally friendly reaction pathways based on the in situ formation of nanoclusters as organic electrosynthesis catalysts.
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