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Electrochemical Radical Formyloxylation–Bromination, −Chlorination, and −Trifluoromethylation of Alkenes

88

Citations

78

References

2019

Year

Abstract

Given the versatility and value of the structurally diverse organohalides and CF<sub>3</sub>-containing compounds in organic synthesis, we reported a green, oxidant-free electrochemical method using undivided electrochemical cells for radical bromination, chlorination and trifluoromethylation-formyloxylation of the various alkenes with readily available halogen radical (NaCl, NaBr), trifluoromethyl radical (CF<sub>3</sub>SO<sub>2</sub>Na) sources, and DMF as formyloxylation reagents. The protocol is operationally simple and robust and the Cl<sup>-</sup>, Br<sup>-</sup> or CF<sub>3</sub><sup>-</sup> was directly oxidized at the anode, obviating the need for exogenous chemical oxidants.

References

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