The key step for the synthesis of 7-hydroxy 2, 3-diarylsubstituted benzothiophenes 5a-f, by starting from substituted 2-aryl-2-((2-methoxy phenyl) thio) acetophenones 3a-f as an intermediate, consists of a Friedel-Crafts cyclization followed by demethylation by Lewis acids like BF 3 OEt 2 and AlCl 3 in DCM.