The transformation of benzothiophene (BT) with 2-methyl-1 -pentene was investigated over HBEA, HMCM-22 and HY zeolites having similar Bronsted acidities, at 85 C under atmospheric pressure in a fixed bed reactor. Over these zeolites. BT underwent only alkylation, whereas 2-methyl-1-pentene underwent alkylation, isomerization and oligomerization. HY was shown to be the most active and stable in BT conversion. HMCM-22 had a low initial activity and a poor stability, due to both diffusional limitations and fast deactivation of its acid sites, even those located in the external pockets. HBEA presented an intermediate behavior. The presence of toluene led to a decrease of BT conversion, which was attributed to competitive adsorptions of the aromatic and the olefin. Whatever the zeolite and the conversion, BT was predominantly transformed into monoalkylated products whereas 3-methylthiophene led essentially to dialkylated products. These results are in agreement with those obtained from theoretical calculations. HMCM-22 zeolite was shown to be the most selective toward alkylation versus olefin oligomerization. (c) 2012 Elsevier B.V. All rights reserved.