“…1 H NMR (400 MHz, CDCl 3 , ppm): 1.41 (t, J = 7.0 Hz, 6H, CH 2 CH 3 ), 3.60 (s, 6H, NCH 3 ), 4.40 (q, J = 7.0 Hz, 4H, CH 2 CH 3 ), 7.3−8.1 (m, 18H, Ph). 13 C NMR (400 MHz, CDCl 3 , ppm): 14.40 (OCH 2 CH 3 ), 41.94 (NCH 3 ), 61.23 (OCH 2 CH 3 ), 124 N-(4-Ethoxycarbonylphenyl)-N-methyl-N′-benzimidoyl Chloride (8). The synthesis of 8 was adopted from the general procedure.…”