2-(4-Nitrophenyl)oxazole → 4-(1,3-Oxazol-2-yl)aniline
Reaktionsgleichung
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[O:11][CH:12]=[CH:13][N:14]=2)=[CH:6][CH:5]=1)([O-])=O>CO.[Pd]>[O:11]1[CH:12]=[CH:13][N:14]=[C:10]1[C:7]1[CH:8]=[CH:9][C:4]([NH2:1])=[CH:5][CH:6]=1Komponenten
4
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A solution of 2-(4-nitro-phenyl)-oxazole (400 mg, 2.1 mmol) in methanol (10 ml) was hydrogenated over 10% Pd/C at 30 psi until no further gas uptake was observed. The reaction mixture was then filtered over celite and concentrated to give a residue which was purified by column chromatography using ethyl acetate/pet ether (3:7) to yield 4-oxazol-2-yl-phenylamine (300 mg, 89%).
Aufarbeitung
- filtrationThe reaction mixture was then filtered over celite and
- concentrationconcentrated
- customto give a residue which
- customwas purified by column chromatography
Quellen und Nachweise
- ORD-Eintrag
- ord-a98a99afd6534c989164d7913d7a956d
- Quelldatensatz
- uspto-grants-2013_07
- Patentnummer
- US08486962B2
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