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An electrochemical synthesis of mono- and 1,1-disubstituted cyclopropanes has been demonstrated. Readily available 1,3-dialkyl bromides were used as starting materials, and the method was enabled by the incorporation of a sacrificial reductant along with cost-effective cathode and anode materials. The need for a divided cell and the use of hazardous or expensive electrodes were eliminated, facilitating the adaptation of the protocol to a continuous flow system. Additionally, an alternative protocol employing a simple sacrificial anode was described.