反应详情

Distilled THF (20 mL) was added to 3-chloro-3-(4-chlorophenyl)-3H-isobenzofuran-1-one (535.4 mg, 1.91 mmol) followed by triethylamine (398.9 mg, 0.549 mL, 3.94 mmol) and n-propylamine (159.8 mg, 0.22 mL, 1.792 mmol). The mixture was stirred at room temperature under nitrogen for 4 hours and monitored by TLC. Upon completion the mixture was then extracted with EtOAc (15 mL) and washed with saturated sodium bicarbonate (3×10 mL), water (3×10 mL) and dried (Na2SO4). Recrysallisation from a minimum amount of boiling ethyl acetate and an excess of petrol yielded the title product as a white crystalline solid (425 mg, 1.409 mmol, 77%). 1H NMR: (300 Hz, CDCl3) δ ppm 0.76 (t, 3H, H11), 1.45 (m, 2H, H10), 2.86 (m, 1H, H9), 3.36 (m, 1H, H9′), 7.16 (d, 1H, H5), 7.38 (dd, 4H, H1-H4), 7.45 (m, 2H, H6-H7), 7.70 (d, 1H, H8). 13C NMR: (75 Hz, DMSO); δ 11.87 (N—CH2—CH2—CH3), 21.96 (N—CH2—CH2), 40.69 (N—CH2), 90.50 (O—C—N), 122.75, 122.99, 128.24, 128.76, 129.58, 131.04, 131.24, 132.73, 133.13, 139.94, 149.59 (Ar), 166.96 (C═O). Mp: 201.5-201.7° C. IR: 1466, 1608, 1664, 2968, 3157 cm−1.

1. distillationDistilled THF (20 mL)
2. extractionUpon completion the mixture was then extracted with EtOAc (15 mL)
3. washwashed with saturated sodium bicarbonate (3×10 mL), water (3×10 mL)
4. dry with materialdried (Na2SO4)