The Fries rearrangement of phenyl acetate, p-tolyl acetate and phenyl
benzoate was investigated using the H-form of various zeolites as cata
lysts. Experiments were carried out in batch reactors at 453 K and for
phenyl acetate at several temperatures both in liquid phase and in ga
s phase in a continuous reactor. Product distribution and catalyst dea
ctivation were strongly dependent on zeolite structure. Deactivation o
f external acidic sites enhanced the yield of para products and improv
ed the selectivity of catalysts based on ZSM-5 and ZSM-12.