Reaktionsgleichung
[F:1][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-])=O)=[CH:4][C:3]=1[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[S:17][CH3:18].O.O.[Sn](Cl)Cl>O1CCCC1.C(O)C>[F:1][C:2]1[CH:7]=[CH:6][C:5]([NH2:8])=[CH:4][C:3]=1[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[S:17][CH3:18]Komponenten
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A solution of 2-fluoro-2′-methylthio-5-nitrobiphenyl (6.00 g, 22.8 mmol) in tetrahydrofuran (50 ml) and ethanol (50 ml) was treated with tin(II) chloride dihydrate (25.70 g, 113.9 mmol) and the mixture was stirred at ambient temperature for 25 h. The solvent was evaporated and the residue stirred with 2N sodium hydroxide solution (240 ml) for 18 h. The resulting suspension was extracted with dichloromethane (3×200 ml). The combined organic extracts were dried over anhydrous magnesium sulphate and evaporated. The residue was purified by flash chromatography on silica gel eluting with 35% ethyl acetate in isohexane to afford 2-fluoro-2′-(methylthio)biphenyl-5-ylamine as a white solid (5.20 g, 98%): δH (360 MHz, CDCl3) 2.39 (3H, s), 6.60 (1H, dd, J 6 and 3), 6.64-6.68 (1H, m), 6.94 (1H, t, J 9), 7.19-7.20 (2H, m), 7.30 (1H, d, J 8), 7.33-7.37 (1H, m).
Aufarbeitung
- customThe solvent was evaporated
- stirringthe residue stirred with 2N sodium hydroxide solution (240 ml) for 18 h
- extractionThe resulting suspension was extracted with dichloromethane (3×200 ml)
- dry with materialThe combined organic extracts were dried over anhydrous magnesium sulphate
- customevaporated
- customThe residue was purified by flash chromatography on silica gel eluting with 35% ethyl acetate in isohexane
Quellen und Nachweise
- ORD-Eintrag
- ord-bb5a349e83484d9982d7f125976cb86c
- Quelldatensatz
- uspto-grants-2005_05
- Patentnummer
- US06900215B2
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