3-Pyridineacrylic acid ethyl ester → Ethyl 3-(piperidin-3-yl)propanoate
Reaktionsgleichung
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH:7]=[CH:8][C:9]([O:11][CH2:12][CH3:13])=[O:10])[CH:2]=1>C(O)C.[Rh]>[NH:1]1[CH2:6][CH2:5][CH2:4][CH:3]([CH2:7][CH2:8][C:9]([O:11][CH2:12][CH3:13])=[O:10])[CH2:2]1Komponenten
4
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A solution of ethyl 3-[pyrid-3-yl]prop-2-enoate (60 g, 0.34 mol) in ethanol (600 ml) was treated with 5% rhodium on alumina powder (17.2 g). The mixture was placed under a hydrogen atmosphere (55 psi) for five hours at 60° C. The reaction was stopped by removing the hydrogen and the reaciton mixture was filtered through a layer of CELITE™. The residue was washed with hot ethanol. The filtrate was concentrated and purified by flash chromatography to provide 39.6 grams (63%) of the desired title product.
Aufarbeitung
- customfor five hours
- customat 60° C
- customby removing the hydrogen
- filtrationthe reaciton mixture was filtered through a layer of CELITE™
- washThe residue was washed with hot ethanol
- concentrationThe filtrate was concentrated
- custompurified by flash chromatography
Quellen und Nachweise
- ORD-Eintrag
- ord-ba1e9b63491444768e7cf975c5aeaf03
- Quelldatensatz
- uspto-grants-1998_07
- Patentnummer
- US05776931
Notizen zur Reaktion
Wird geladen…