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
- 65 °C
PROCEDURE
实验过程
150 g (2R,4S)-5-biphenyl-4-yl-4-tert-butoxycarbonylamino-2-methylpentanoic acid (3-a, R1=BOC, R2=R3=H) are added to 1500 ml ethanol at room temperature. The mixture is then warmed to an internal temperature of 60-70° C. 42.8 ml Thionyl chloride is then added over a period of 1 h to the reaction mixture. The mixture is then stirred for a further 2 h. 810 ml of the solvent is removed by distillation under reduced pressure. 1460 ml Heptane fraction is then added. 1310 ml of solvent is then removed by distillation under reduced pressure. 1460 ml Heptane fraction is then added. 520 ml of solvent is then removed by distillation under reduced pressure. 1460 ml Heptane fraction is then added. The mixture is then cooled to room temperature over a period of 1 h. The mixture is then stirred at room temperature for 2 h. The solid is then collected by filtration. The solid is then washed with heptane fraction (600 ml) and dried to give (2R,4S)-4-amino-5-biphenyl-4-yl-2-methylpentanoic acid ethyl ester hydrochloride (3-a, R1=R2=H, R3=Et). Spectroscopic data as given in Example 9-1 Method 1.
WORKUP
后处理
- custom810 ml of the solvent is removed by distillation under reduced pressure
- addition1460 ml Heptane fraction is then added
- custom1310 ml of solvent is then removed by distillation under reduced pressure
- addition1460 ml Heptane fraction is then added
- custom520 ml of solvent is then removed by distillation under reduced pressure
- addition1460 ml Heptane fraction is then added
- temperatureThe mixture is then cooled to room temperature over a period of 1 h
- stirringThe mixture is then stirred at room temperature for 2 h
- filtrationThe solid is then collected by filtration
- washThe solid is then washed with heptane fraction (600 ml)
- customdried