3-(4-Methoxypyridin-2-yl)-nitrobenzene → 3-(4-Methoxypyridin-2-yl)aniline
Reaktionsgleichung
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][N:6]=[C:5]([C:9]2[CH:10]=[C:11]([N+:15]([O-])=O)[CH:12]=[CH:13][CH:14]=2)[CH:4]=1>C(O)C.[Pd]>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][N:6]=[C:5]([C:9]2[CH:10]=[C:11]([CH:12]=[CH:13][CH:14]=2)[NH2:15])[CH:4]=1Komponenten
4
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A suspension of 3-(4-methoxypyridin-2-yl)nitrobenzene (1.8 g) in ethanol (40 ml) was hydrogenated over palladium on carbon (10% w/w, 50% wet, 800 mg) under a hydrogen atmosphere for 5 hours. The catalyst was filtered off, and the filtrate was evaporated under reduced pressure to give 3-(4-methoxypyridin-2-yl)aniline (1.57 g).
Aufarbeitung
- filtrationThe catalyst was filtered off
- customthe filtrate was evaporated under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-61a70675b81949c597523928ecb22736
- Quelldatensatz
- uspto-grants-2003_02
- Patentnummer
- US06521643B1
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