“…12 On the other hand, organic electrochemistry, which drives redox processes with electric current, has been proven to be a powerful synthetic tool in organic chemistry due to its prominent advantages, namely mild reaction conditions, easy reaction process control, high material utilization, and low energy consumption. 13 As part of our efforts to continuously develop cheap and eco-friendly catalytic methods under electrochemical conditions, 14 we herein describe the electrocatalytic ring-opening dihydroalkoxylation of N -aryl maleimides with alcohols under metal- and oxidant-free conditions. This electrochemical process consists of anodic single-electron transfer oxidation, cathodic radical reduction, rearrangement-ring cleavage and nucleophilic addition cascade, which employs tetrabutylammonium bromide not only as a redox catalyst but also as an efficient supporting electrolyte, and offers a practical and environmentally friendly route to ring-opening dihydroalkoxylation products (Scheme 1c).…”