Reaktionsgleichung
[N:1]1[C:9]2[CH2:8][CH2:7][CH2:6][C:5]=2[CH:4]=[CH:3][CH:2]=1.[CH:10](=O)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.C(OC(=O)C)(=O)C>>[CH:10](=[C:8]1[C:9]2[N:1]=[CH:2][CH:3]=[CH:4][C:5]=2[CH2:6][CH2:7]1)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1Komponenten
4
Versuchsvorschrift
15 g (0.125 mol) of 6,7-dihydro-5H-[1]pyrindine, 20.1 g (0.19 mol) of freshly destilled benzaldehyde and 24.5 g (0.24 mol) of acetic acid anhydride were heated under reflux for 24 h. The reaction mixture was evaporated, the residual oil dissolved in methylene chloride, the solution extracted with 1N NaOH solution, and the organic phase dried and evaporated. The residue was destilled under reduced pressure to give 19.3 g (75%) of the title compound.
Aufarbeitung
- temperatureunder reflux for 24 h
- customThe reaction mixture was evaporated
- dissolutionthe residual oil dissolved in methylene chloride
- extractionthe solution extracted with 1N NaOH solution
- customthe organic phase dried
- customevaporated
Quellen und Nachweise
- ORD-Eintrag
- ord-b4246cd9d8eb40b4b6de6d466dbf1014
- Quelldatensatz
- uspto-grants-2006_09
- Patentnummer
- US07105513B2
Verknüpfte Notizen
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