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
- -78 °C
PROCEDURE
实验过程
A colourless solution of (3-bromo-2-methylphenethoxy)(tert-butyl)dimethylsilane [Aromatic Intermediate 22, step c] (2.06 g) in THF (40 mL) was cooled to −78° C. under an atmosphere of nitrogen and treated with butyllithium (2.1M in hexanes, 3.3 mL), added dropwise over 3 minutes. The resulting pale yellow solution was stirred at −78° C. for 30 minutes, treated with N,N-dimethylformamide (0.73 mL) added dropwise over 2 minutes to give a colourless solution, stirred at −78° C. for a further 30 minutes, then removed from the cooling bath and allowed to warm to room temperature over 45 minutes. The solution was quenched by the addition of 10% aqueous ammonium chloride (100 mL), and the resulting mixture was extracted twice with diethyl ether. The combined organic phases were washed with brine, dried over anhydrous magnesium sulphate and concentrated in vacuo to afford the titled compound as a pale yellow oil. Yield 1.74 g.
WORKUP
后处理
- additionadded dropwise over 3 minutes
- additionadded dropwise over 2 minutes
- customto give a colourless solution
- stirringstirred at −78° C. for a further 30 minutes
- customremoved from the cooling bath
- temperatureto warm to room temperature over 45 minutes
- customThe solution was quenched by the addition of 10% aqueous ammonium chloride (100 mL)
- extractionthe resulting mixture was extracted twice with diethyl ether
- washThe combined organic phases were washed with brine
- dry with materialdried over anhydrous magnesium sulphate
- concentrationconcentrated in vacuo