反应详情

To a solution of 2,2,-bis-difluoromethyl-2-hydroxy-acetic acid (1.76 g, 10 mmole) in tetrahydrofuran(40ml) was added carbonyl diimidazole (0.81 g, 5 mmole). The flask was placed in a sonic bath and the reaction sonicated for 20 minutes followed by addition of 4-aminobenzophenone. The reaction was sonicated for 18 hours. The reaction mixture was filtered and the liltrate evaporated to dryness. The recovered pasty solid was washed with ether and the combined ether washinEs evaporated. The recovered solid was crystallized from ethyl acetate/hexane to give the title compound (0.89 g, 25%) as yellow crystals; mp 139°-142° C. 1H-NMR (300 HHz, d6 -DHSO): 6.48(t, J=53.7 Hz, 2H, HCF2); 7.53-7.77 (m, 7H, ArH, OH); 7.95-7.98(m, 3H, ArH); 10.43 (s, 1H, NH). MS(CI,CH4): 356(H+1, 100%).

1. customThe flask was placed in a sonic bath
2. customthe reaction sonicated for 20 minutes
3. customThe reaction was sonicated for 18 hours
4. filtrationThe reaction mixture was filtered
5. customthe liltrate evaporated to dryness
6. washThe recovered pasty solid was washed with ether
7. customthe combined ether washinEs evaporated
8. customThe recovered solid was crystallized from ethyl acetate/hexane