The functional group compatibility of an electrosynthetic
method
is typically limited by its potential reaction window. Here, we report
that alternating current (AC) electrolysis can overcome such potential
window-limited functional group compatibility. Using alkene heterodifunctionalization
as a model system, we design and demonstrate a series of AC-driven
reactions that add two functional groups sequentially and separately
under the cathodic and anodic pulses, including chloro- and bromotrilfuoromethylation
as well as chlorosulfonylation. We discovered that the oscillating
redox environment during AC electrolysis allows the regeneration of
the redox-active functional groups after their oxidation or reduction
in the preceding step. As a result, even though redox labile functional
groups such as pyrrole, quinone, and aryl thioether fall in the reaction
potential window, they are tolerated under AC electrolysis conditions,
leading to synthetically useful yields. The cyclic voltammetric study
has confirmed that the product yield is limited by the extent of starting
material regeneration during the redox cycling. Our findings open
a new avenue for improving functional group compatibility in electrosynthesis
and show the possibility of predicting the product yield under AC
electrolysis from voltammogram features.