反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
CONDITIONS
反应条件
- 温度
- 200 °C
PROCEDURE
实验过程
A 1-liter capacity flask equipped with N2 -bleeding tube, thermometer, paddle stirrer, and condenser was charged with 2-phenyl-4-quinolinecarboxylic acid, 227.7 g (0.90 mol), quinoline 200.0 g, and cupurons oxide 20.0 g (0.14 mol). The flask was heated with stirring to 200° C., and maintained at 200° C. for 1 hour. CO2 started to evolve at about 120° C. The mixture was cooled to room temperature, and filtered by suction using filter aid and ether. Ether was evaporated from the filtrate in a vacuum evaporator, and the residue was subjected to fractional distillation under vacuum. A fraction was collected at 140° C./0.2 mmHG-155° C./0.5 mmHg which was 99+% pure 2-phenylquinoline by GC, NMR. M.p. 80°-84° C. The yield was 82.0 g (44%).
WORKUP
后处理
- customA 1-liter capacity flask equipped with N2 -bleeding tube
- temperatureThe flask was heated
- temperaturemaintained at 200° C. for 1 hour
- customto evolve at about 120° C
- temperatureThe mixture was cooled to room temperature
- filtrationfiltered by suction
- filtrationusing filter aid and ether
- customEther was evaporated from the filtrate in a vacuum evaporator
- distillationthe residue was subjected to fractional distillation under vacuum
- customA fraction was collected at 140° C./0.2 mmHG-155° C./0.5 mmHg which