Notes J. Org. Chem., Vol. 53, No. 1, 1988 213 chloride/dimethyl formamide) to produce the corresponding chloroaldehyde 2a or 2b in 7540% yield (Scheme I). The resulting chloroaldehyde 2a or 2b was treated with aniline or p-methoxyaniline in ethanol to get the anil derivative 3a or 3b in 85-90% yield. The anil derivative 3a or 3b on brief heating at 250" C readily cyclized to dihydrobenz [c] acridine 4a5 or 4b as the only isolable product in 65- ...