4-Chlorobenzaldehyde → 5-(4-chlorophenyl)-5H,6aH-benzo[4,5][1,3]oxazino[3,2-a]quinoline

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Reaktionsschritte

Following the general procedure, treatment of 8-methoxyquinoline (0.086 g, 0.50 mmol) and 4-chlorobenzaldehyde (0.105 g, 0.75 mmol) with 2-(trimethylsilyl)phenyl trifluoromethanesulfonate (0.179 g, 146 μL, 0.60 mmol) in the presence of KF (0.070 g, 1.2 mmol) and 18-crown-6 (0.317 g, 1.2 mmol) in THF (2.0 mL) at −10° C. to room temperature for 12 hrs followed by flash column chromatography (Pet. ether/EtOAc=70/30) of the crude reaction mixture afforded 5-(4-chlorophenyl)-5H,6aH-benzo[4,5][1,3]oxazino[3,2-a]quinoline as inseparable mixture of diastereomers as a white solid (0.121 g, 65% yield, dr determined by 1H NMR analysis of crude reaction mixture is 1:1).

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