反应详情

A suspension of 22.8 g (64.2 mmol) of 1-(4-methoxy-benzyl)-4-(4-nitro-phenyl)-piperidine-2,6-dione (as prepared in the previous step) in CH3CN (150 mL) was treated with 70.4 g (128 mmol) of ceric ammonium nitrate (CAN) as a solution in water (100 mL). The mixture was stirred at RT for 5 h, diluted with water (100 mL), and extracted with EtOAc (2×150 mL). The combined organic layers were washed with saturated aqueous NaHCO3 (1×100 mL) and water (1×100 mL). The combined aqueous layers were extracted with EtOAc (1×100 mL). The combined organic layers were dried (MgSO4) and concentrated in vacuo. The solid residue was triturated with a minimum amount of CH3CN, filtered, and air-dried. The filtrate was concentrated and triturated again with a minimum amount of CH3CN, filtered, and air-dried as a second batch. The two batches were combined to afford 7.00 g (47%) as an off-white solid: 1H-NMR (CDCl3; 400 MHz): δ 8.26 (d, 2H, J=8.8 Hz), 7.97 (br s, 1H), 7.42 (d, 2H, J=8.8 Hz), 3.62-3.52 (m, 1H), 3.02-2.93 (m, 2H), 2.84-2.74 (m, 2H).

1. extractionextracted with EtOAc (2×150 mL)
2. washThe combined organic layers were washed with saturated aqueous NaHCO3 (1×100 mL) and water (1×100 mL)
3. extractionThe combined aqueous layers were extracted with EtOAc (1×100 mL)
4. dry with materialThe combined organic layers were dried (MgSO4)
5. concentrationconcentrated in vacuo
6. customThe solid residue was triturated with a minimum amount of CH3CN
7. filtrationfiltered
8. customair-dried
9. concentrationThe filtrate was concentrated
10. customtriturated again with a minimum amount of CH3CN
11. filtrationfiltered
12. customair-dried as a second batch
13. customto afford 7.00 g (47%) as an off-white solid