1-(5-Ethoxy-2-nitrophenyl)piperidine → 4-Ethoxy-2-(piperidin-1-yl)aniline
Reaktionsgleichung
[CH2:1]([O:3][C:4]1[CH:5]=[CH:6][C:7]([N+:16]([O-])=O)=[C:8]([N:10]2[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]2)[CH:9]=1)[CH3:2]>[Pd]>[CH2:1]([O:3][C:4]1[CH:5]=[CH:6][C:7]([NH2:16])=[C:8]([N:10]2[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]2)[CH:9]=1)[CH3:2]Komponenten
3
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Using a procedure similar to Example 3, step (c), 1-(5-ethoxy-2-nitro-phenyl)-piperidine (78 mg, 0.31 mmol, as prepared in the previous step) was stirred with 42 mg of 5% Pd—C under H2 to afford 64 mg (94%) of the title compound which was used immediately without further purification. Mass spectrum (ESI, m/z): Calcd. for C13H20N2O, 221.1 (M+H), found 221.1.
Aufarbeitung
- customas prepared in the previous step)
Quellen und Nachweise
- ORD-Eintrag
- ord-ef5c8e283cba49eca3085d263703a51f
- Quelldatensatz
- uspto-grants-2008_09
- Patentnummer
- US07427683B2
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