Table 7: 1H NMR Data for 4a-f; chemical shifts in ppm relative to TMS(1%) at room temperature in CDCl3.

No. X Aromatic Ha Hb CH2 CH3 X
4a p-CN 7.11(2H,d,J=7.8Hz) 3.84(4H,br) 2.56(4H,br) 3.51(2H,s) 2.31(3H,s)
7.19(2H,d,J=7.9Hz)
7.43(2H,d,J=8.6Hz)
7.55(2H,d,J=8.6Hz)
7.12(2H,d,J=7.8Hz)
4b p-CO2CH3 7.20(2H,d,J=7.9Hz) 3.83(4H,t, 2.56(4H,t, 3.51(2H,s) 2.32(3H,s) 3.86(3H,s)
7.43(2H,d,J=8.5Hz)
7.98(2H,d,J=8.5Hz) J=5.2Hz) J=6.3Hz)
7.11(2H,d,J=7.8Hz)
4c p-Br 7.19(2H,d,J=7.9Hz) 3.76(4H,t, 2.55(4H,t, 3.51(2H,s) 2.31(3H,s)
7.27(2H,d,J=8.8Hz)
7.40(2H,d,J=8.7Hz) J=5.3Hz) J=5.2Hz)
7.13(2H,d,J=8.0Hz)
4d p-CH3 7.14(2H,d,J=7.4Hz) 3.76(4H,t, 2.57(4H,t, 3.53(2H,s) 2.33(3H,s) 2.34(3H,s)
7.23(2H,d,J=8.0Hz)
7.33(2H,d,J=8.3Hz) J=5.3Hz) J=5.2Hz)
7.12(2H,d,J=7.9Hz)
4e p-NO2 7.20(2H,d,J=7.9Hz) 3.88(4H,br) 2.58(4H,br) 3.52(2H,s) 2.32(3H,s)
7.47(2H,d,J=9.1Hz)
8.16(2H,d,J=9.1Hz)
4f H 7.22(2H,d,J=7.9Hz) 3.78(4H,t, 2.58(4H,t, 3.53(2H,s) 2.34(3H,s)
7.32(2H,t,J=7.8Hz)
7.41(2H,d,J=8.2Hz) J=5.2Hz) J=5.2Hz)
7.17-7.13(3H,m)