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
- 2.5 °C
PROCEDURE
实验过程
33 ml of lithium diisopropylamide solution (1 M in THF) are initially introduced at 0° C. under nitrogen, and a solution of 3.6 g of 3-methylpyridine 1 in 50 ml of THF is added dropwise with stirring at 0-5° C. The mixture is stirred for a further 30 minutes at the temperature indicated, and a solution of 5 g of 3,4,5-trimethoxybenzonitrile in 50 ml of THF is subsequently added. The mixture is stirred at 0-5° C. for a further 1.5 h, and finally a further 33 ml of lithium diisopropylamide solution are added. The reaction mixture is subsequently warmed at 80° C. for 2 h. For work-up, the batch is allowed to cool to room temperature, and the mixture is poured onto ice. After phase separation, the mixture is extracted a further three times with 100 ml of dichloromethane each time, the combined organic phases are dried, and the solvent is removed in vacuo. The residue is purified by chromatography over a silica-gel column using ethyl acetate, giving 4.3 g of yellow crystals, which exhibit a melting point of 174.0-175.5° C.
WORKUP
后处理
- stirringThe mixture is stirred for a further 30 minutes at the temperature
- stirringThe mixture is stirred at 0-5° C. for a further 1.5 h
- temperatureThe reaction mixture is subsequently warmed at 80° C. for 2 h
- temperatureto cool to room temperature
- additionthe mixture is poured onto ice
- customAfter phase separation
- extractionthe mixture is extracted a further three times with 100 ml of dichloromethane each time
- customthe combined organic phases are dried
- customthe solvent is removed in vacuo
- customThe residue is purified by chromatography over a silica-gel column