Abstract
Paired electrosynthesis, which utilize both anodic and cathodic events in electrolysis,
enables attractive transformations with higher current efficiency than conventional
electrosynthesis. The electrochemical flow technique has been widely employed to ensure
stable reaction conditions and mitigate issues stemming from mass transfer. In this
study, the electrochemical Meinwald rearrangement of styrene oxides was investigated,
yielding aldehydes as intermediates, followed by the nitromethylation of aldehydes
to produce β-nitro alcohols. These reactions were achieved with catalytic electrical
input, enabling the conversion of various styrene oxides into the corresponding β-nitro
alcohols.
Key words electrochemical organic synthesis - paired electrolysis - Meinwald rearrangement -
nitromethylation - flow synthesis