The kinetics of liquid-phase reduction of 2-chloro-4-nitroaniline on p
latinum and palladium catalysts with a varied content of the metals is
studied. Hydrodehalogenation is found to occur as a side reaction. Th
e effect of various factors on the rate and selectivity of the process
is examined. It is shown that hydrodehalogenation involves essentiall
y the initial nitro compound. The main and side processes are the para
llel first-order reactions. The decrease in the rate constants of the
main and side reactions in a series of aliphatic alcohols correlates w
ell with weakening electrophilic properties of the solvents. Optimum c
onditions, which ensure the high rate and selectivity of the reaction,
are selected.