HRID564470

反应详情

EQUATION

反应方程式

HRID 564470 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

TBSCl (18.7 g, 124.3 mmol), Et3N (14.08 g, 139.2 mmol) and DMAP (194.3 mg, 8.9 mmol) were dissolved in CH2Cl2 (120 mL), then the solution was cooled to 0-5° C. (3-bromophenyl)methanol (18.5 g, 99.4 mmol) was added dropwise to the solution. After the addition, the mixture was warmed to room temperature, and stirred for 2 h. 5% HCl was added to the reaction mixture to pH=4-5, then the organic phase was separated, and the aqueous layer was extracted with CH2Cl2 (50 mL×2). The combined organic phase was washed with water, and dried over Na2SO4. After removing the solvent, 28.5 g of {[(3-Bromophenyl)methyl]oxy}(1,1-dimethylethyl)dimethylsilane was obtained (Yield: 95.1%).

WORKUP

后处理

  1. additionwas added dropwise to the solution
  2. additionAfter the addition
  3. customthe organic phase was separated
  4. extractionthe aqueous layer was extracted with CH2Cl2 (50 mL×2)
  5. washThe combined organic phase was washed with water
  6. dry with materialdried over Na2SO4
  7. customAfter removing the solvent