Stannous chloride dihydrate → HCID 22285321, compound

Reaction equation

[F:1][C:2]1[CH:3]=[C:4]([C:11]2[C:12]([C:17]#[N:18])=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH:5]=[C:6]([N+:8]([O-])=O)[CH:7]=1.O.O.[Sn](Cl)Cl>C(O)C.O1CCCC1>[NH2:8][C:6]1[CH:7]=[C:2]([F:1])[CH:3]=[C:4]([C:11]2[C:12]([C:17]#[N:18])=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH:5]=1

Participants

Procedure

A cooled (0° C.) suspension of 3′-fluoro-5′-nitrobiphenyl-2-carbonitrile (8.9 g, 37 mmol) in ethanol (70 mL) and tetrahydrofuran (70 mL) was treated with tin(II) chloride dihydrate (29 g, 129 mmol) and the mixture was stirred at ambient temperature for 4 h. The solvent was removed in vacuo and the residue treated with ice-cold 2 N sodium hydroxide (400 mL). The resulting slurry was stirred for 30 min then extracted with dichloromethane (2×400 mL). The organics were combined, washed with water and brine, dried over anhydrous magnesium sulfate, filtered and pre-adsorbed onto silica. Purification by dry flash chromatography on silica, eluting with dichloromethane containing 0.5% triethylamine, afforded 5′-amino-3′-fluorobiphenyl-2-carbonitrile as a white solid (4.5 g, 58%): δH (400 MHz, CDCl3) 3.90 (2H, br), 6.45 (1H, ddd, J 8, 2 and 2), 6.58-6.63 (2H, m), 7.44 (1H, ddd, J 8, 8 and 2), 7.48 (1H, dd, J 8 and 2), 7.62 (1H, ddd, J 8, 8 and 2), 7.74 (1H, dd, J 8 and 2).