HRID257493

反应详情

EQUATION

反应方程式

HRID 257493 的结构方程式

PROCEDURE

实验过程

In a flask, 0.61 g (18 mmol) of lithium aluminum hydride and 50 ml of dried tetrahydrofuran were placed. While cooling with ice-cold water under a nitrogen atmosphere, a solution of 10.0 g (82.6 mmol) of 4-isopropylpyridine dissolved in tetrahydrofuran was added dropwise. After stirring for 24 hours at room temperature, a solution of 3.41 g (16.0 mmol) of 4-phenylbutyl bromide dissolved in tetrahydrofuran was added. The resulting mixture was stirred for 2 hours. Subsequently, water was added, tetrahydrofuran was distilled away under reduced pressure, and then the residue was extracted with ethyl acetate. After the extract was dried over anhydrous sodium sulfate, ethyl acetate was distilled away under reduced pressure. The resulting oily substance was purified by silica gel column chromatography, to obtain 0.21 g (yield: 5.2%) of the desired compound.

WORKUP

后处理

  1. temperatureWhile cooling with ice-cold water under a nitrogen atmosphere
  2. additionwas added dropwise
  3. additionwas added
  4. stirringThe resulting mixture was stirred for 2 hours
  5. distillationtetrahydrofuran was distilled away under reduced pressure
  6. extractionthe residue was extracted with ethyl acetate
  7. dry with materialAfter the extract was dried over anhydrous sodium sulfate, ethyl acetate
  8. distillationwas distilled away under reduced pressure
  9. customThe resulting oily substance was purified by silica gel column chromatography