cis-N-[3-(3-pyridyl)cyclohexyl]phthalimide → cis-3-(3-Pyridyl)cyclohexylamine
Reaktionsgleichung
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C@@H:7]2[CH2:12][CH2:11][CH2:10][C@H:9]([N:13]3C(=O)C4=CC=CC=C4C3=O)[CH2:8]2)[CH:2]=1>CCO>[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C@@H:7]2[CH2:12][CH2:11][CH2:10][C@H:9]([NH2:13])[CH2:8]2)[CH:2]=1Komponenten
3
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of cis-N-[3-(3-pyridyl)cyclohexyl]phtalimide (1.64 g, 5.35 mmol) and hydrazinemonohydorate (0.52 mL, 10.7 mmol) in EtOH (25 mL) was stirred at room temperature for 2 h. The reaction mixture was filtered followed by the removal of solvent. The crude product was purified by column chromatography (NH, EtOAc) to yield cis-3-(3-pyridyl)cyclohexylamine (348 g, 37%) as colorless oil.
Aufarbeitung
- filtrationThe reaction mixture was filtered
- customfollowed by the removal of solvent
- customThe crude product was purified by column chromatography (NH, EtOAc)
Quellen und Nachweise
- ORD-Eintrag
- ord-3d83ef17f8a24d90af4e87a4c80cbbfe
- Quelldatensatz
- uspto-grants-2011_12
- Patentnummer
- US08071591B2
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