Stannous chloride dihydrate → 5'-Amino-2'-fluorobiphenyl-2-carbonitrile
反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-])=O)=[CH:4][C:3]=1[C:11]1[C:12]([C:17]#[N:18])=[CH:13][CH:14]=[CH:15][CH:16]=1.O.O.[Sn](Cl)Cl>C1COCC1.C(O)C>[NH2:8][C:5]1[CH:6]=[CH:7][C:2]([F:1])=[C:3]([C:11]2[C:12]([C:17]#[N:18])=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH:4]=1参加物
実験手順
To a stirred suspension of 2′-fluoro-5′-nitrobiphenyl-2-carbonitrile (18.71 g, 77.2 mmol) in THF (150 ml) and ethanol (150 ml) was added tin(II) chloride dihydrate (52.42 g, 232.4 mmol) and the mixture was stirred at room temperature for 22.5 h. The mixture was evaporated in vacuo and the residue was treated with ice-cold 2 N aqueous NaOH (800 ml). The resulting mixture was stirred for 1.5 h, then extracted with dichloromethane (2×800 ml). The combined organic extracts were washed with saturated aqueous NaCl (200 ml), dried (MgSO4), and evaporated in vacuo. The residue was recrystallised from hot toluene (100 ml) to afford 11.33 g (69%) of 5′-amino-2′-fluorobiphenyl-2-carbonitrile as a white solid: 1H NMR (360 MHz, CDCl3) δ 3.65 (2H, br s), 6.67-6.73 (2H, m), 7.00 (1H, t, J 9.0 Hz), 7.46 (1H, td, J 7.6, 1.1 Hz), 7.49 (1H, d, J 7.4 Hz), 7.64 (1H, td, J 7.7, 1.3 Hz), 7.76 (1H, dd, J 7.7, 0.7 Hz).
後処理
- customThe mixture was evaporated in vacuo
- additionthe residue was treated with ice-cold 2 N aqueous NaOH (800 ml)
- stirringThe resulting mixture was stirred for 1.5 h
- extractionextracted with dichloromethane (2×800 ml)
- washThe combined organic extracts were washed with saturated aqueous NaCl (200 ml)
- dry with materialdried (MgSO4)
- customevaporated in vacuo
- customThe residue was recrystallised from hot toluene (100 ml)
出典と根拠
- ORDレコード
- ord-52d3ac3165814f71933d945924fe5af4
- 出典データセット
- uspto-grants-2005_08
- 特許番号
- US06936608B2
反応ノート
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