N,N-Diethylaniline → 2-Chloro-5,6,7,8-tetrahydroquinoline
Reaktionsgleichung
O[C:2]1[CH:11]=[CH:10][C:9]2[CH2:8][CH2:7][CH2:6][CH2:5][C:4]=2[N:3]=1.CCN(C1C=CC=CC=1)CC.P(Cl)(Cl)([Cl:25])=O>>[Cl:25][C:2]1[CH:11]=[CH:10][C:9]2[CH2:8][CH2:7][CH2:6][CH2:5][C:4]=2[N:3]=1Komponenten
4
Versuchsvorschrift
A solution of 0.7 g of 2-hydroxy-5,6,7,8-tetrahydroquinoline (prepared according to the methods outlined by Meyers et al., J. Org. Chem., 29: 1435-1438, 1964) and 0.1 g of diethylaniline in 7 mL of phosphorus oxychloride is refluxed for 2 h, cooled and concentrated. The residue taken is up in chloroform, washed with excess 3 N NaOH solution and the organic layer dried and concentrated to provide crude 2-chloro-5,6,7,8-tetrahydro-quinoline (0.45 g) as an oil.
Aufarbeitung
- temperaturecooled
- concentrationconcentrated
- washwashed with excess 3 N NaOH solution
- customthe organic layer dried
- concentrationconcentrated
Quellen und Nachweise
- ORD-Eintrag
- ord-90a92063a867423ea5f4b8a2dbbf63d7
- Quelldatensatz
- uspto-grants-2002_05
- Patentnummer
- US06384224B2
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