反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 85 °C
PROCEDURE
实验过程
To a stirring solution of 3-bromo-propanol (5.9 mL, 65.4 mmol) in acetonitrile (500 ml) was added Nal (19.6 g, 131 mmol) and K2CO3 (18.1 g, 131 mmol). The mixture was stirred at 85° C. for 1 h, and then N-(2,2-diphenylethyl)-N-(2-chloro-3-trifluoromethyl-benzyl)amine (34.0 g, 87.2 mmol) was added. The reaction mixture was heated at 85° C. overnight. Solvent was removed, the residue was washed with H2O, and extracted twice with EtOAc. The EtOAc extracts were dried over Na2SO4, filtered, and concentrated. The crude mixture was purified by silica gel chromatography (35 g Redisep column, silica, 40 um, 60 Å, 35 mL/min, A: hexanes, B: EtOAc, B: 0% for 2 min, B: 0% to 10% over 10 min; B: 10% for 2 min; B: 10% to 20% over 15 min; B: 20% for 2 min; B: 20% to 30% over 40 min; detection at 214 nm) to give 13.3 g (29.7 mmol, 34%) of the title compound as a white solid. 1H NMR (CDCl3, 400 MHz) □: 7.6 (d, J=7.6 Hz, 1H), 7.3-7.1 (m, 12H), 4.2 (t, J=7.6 Hz, 1H), 3.8 (s, 2H), 3.6 (t, J=5.6 Hz, 2H), 3.2 (d, J=7.6 Hz, 2H), 2.8 (t, J=6.0 Hz, 2H), 2.5 (s, 1H), 1.7 (m, 2H);
WORKUP
后处理
- temperatureThe reaction mixture was heated at 85° C. overnight
- customSolvent was removed
- washthe residue was washed with H2O
- extractionextracted twice with EtOAc
- dry with materialThe EtOAc extracts were dried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
- customThe crude mixture was purified by silica gel chromatography (35 g Redisep column, silica, 40 um, 60 Å, 35 mL/min
- waitA: hexanes, B: EtOAc, B: 0% for 2 min
- waitB: 0% to 10% over 10 min
- waitB: 10% for 2 min
- waitB: 10% to 20% over 15 min
- waitB: 20% for 2 min
- waitB: 20% to 30% over 40 min