HRID1255276

反应详情

EQUATION

反应方程式

HRID 1255276 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

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

  1. additionadded dropwise over 3 minutes
  2. additionadded dropwise over 2 minutes
  3. customto give a colourless solution
  4. stirringstirred at −78° C. for a further 30 minutes
  5. customremoved from the cooling bath
  6. temperatureto warm to room temperature over 45 minutes
  7. customThe solution was quenched by the addition of 10% aqueous ammonium chloride (100 mL)
  8. extractionthe resulting mixture was extracted twice with diethyl ether
  9. washThe combined organic phases were washed with brine
  10. dry with materialdried over anhydrous magnesium sulphate
  11. concentrationconcentrated in vacuo