Abstract
1-(p-Chlorobenzoyl)-2-methyl-5-methoxy-3-indoleacetic acid, a potent antiinflammatory drug, was directly prepared from N1-(p-chlorobenzoyl)-p-methoxyphenyl-hydrazine hydrochloride and levulinic acid in excellent yield by the new method. The recrystallization of l-(p-chlorobenzoyl)-2-methyl -5-methoxy-3-indoleacetic acid from solvents gave crystals of polymorphism [alpha], [beta]-, and gamma-types.