HRID35818

反应详情

EQUATION

反应方程式

HRID 35818 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

2.0 of 2-(4,6-dimethoxypyrimidin-2-yl)-3-methyl-N-methylsulfonylbutyric acid amide was placed in a round bottom flask, and was dissolved in 50 ml of DMF. To the resultant solution, was gradually added 0.28 g of 60% sodium hydride, and the mixture was stirred at room temperature for one hour. Thereafter, 1.0 g of chloromethyl ethyl ether was added dropwise to the resultant mixture, and the mixture was stirred at room temperature for 2 hours. The reaction mixture was then poured into ice water, and was extracted with 200 ml of diethyl ether, followed by drying with anhydrous sodium sulfate. After filtrating the inorganic salt, the solvent was distilled off under reduced pressure. An only product thus obtained was purified by silica gel column chromatography (developing solvent: N-hexane/ethyl acetate=10/1) to obtain 1.8 g of the aimed product of colorless transparent viscous liquid (yield=78.3%) having a refractive index (n20/D) of 1.4976.

WORKUP

后处理

  1. stirringthe mixture was stirred at room temperature for 2 hours
  2. extractionwas extracted with 200 ml of diethyl ether
  3. dry with materialby drying with anhydrous sodium sulfate
  4. filtrationAfter filtrating the inorganic salt
  5. distillationthe solvent was distilled off under reduced pressure
  6. customAn only product thus obtained
  7. customwas purified by silica gel column chromatography (developing solvent: N-hexane/ethyl acetate=10/1)