反应详情

3,2′-Difluoro-5′-nitrobiphenyl-2-carbonitrile (3.25 g, 12.5 mmol) in tetrahydrofuran (20 mL) and ethanol (20 mL) was treated with tin(II) chloride dihydrate (9.86 g, 43.8 mmol) and the mixture left to stir at ambient temperature for 18 h. The solvent was evaporated and the residue stirred with 2 N sodium hydroxide solution (40 mL) for 2 h. The resulting suspension was diluted with water (100 mL) and extracted with dichloromethane (3×200 mL). The combined organics were washed with water (200 mL), brine (200 mL), dried over anhydrous sodium sulfate, filtered and evaporated to give 5′-amino-3,2′-difluorobiphenyl-2-carbonitrile as a brown solid (2.87 9, 100%): δH (360 MHz, CDCl3) 3.74 (2H, s), 6.66-6.75 (2H, m), 7.01 (1H, dd, J 9 and 9), 7.19-7.30 (2H, m), 7.59-7.65 (1H, m).

1. waitthe mixture left
2. customThe solvent was evaporated
3. stirringthe residue stirred with 2 N sodium hydroxide solution (40 mL) for 2 h
4. additionThe resulting suspension was diluted with water (100 mL)
5. extractionextracted with dichloromethane (3×200 mL)
6. washThe combined organics were washed with water (200 mL), brine (200 mL)
7. dry with materialdried over anhydrous sodium sulfate
8. filtrationfiltered
9. customevaporated