751-757The electrochemical reduction of benzyl bromide
has been investigated in acetonitrile and CO2-saturated acetonitrile
by cyclic voltammetry and contro lled-potential electrolysis. Electroreduction of
the halide in the absence of CO2 leads to a variety of products, the
distribution of which depends on the elec trode material, applied potential
and proton availability in the medium. The electrocarboxylation process, have been
carried out at Hg and graphite cathodes using both a two compartment cell and an
undivided cell with dissolving Al anode. The best results (87% phenylacetic yield)
are obtained at Hg in the undivided cell. Catalysis by Co(salen) allows the process
to be performed at potentials more positive than those required by direct reduction
but gives only poor to moderate yields of acid. Results obtained from experiments
carried out
with benzyl chloride have been compared with
those obtained in the case of benzyl bromide