反应详情

Following the general procedure, treatment of quinoline (0.064g, 59 μL, 0.50 mmol) and 4-methoxybenzaldehyde (0.136 g, 91 μL, 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 rt for 12 h followed by flash column chromatography (Pet. ether/EtOAc=75/25) of the crude reaction mixture afforded 5-(4-methoxyphenyl)-5H,6aH-benzo[4,5][1,3]oxazino[3,2-a]quinoline as a yellow solid (0.112 g, 66% yield, dr determined by 1H NMR analysis of crude reaction mixture is >20:1).

1. customat −10° C. to rt
2. customfor 12 h
3. customreaction mixture