HRID64985

反应详情

EQUATION

反应方程式

HRID 64985 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

14.7 g (0.10 mole) of p-methoxyphenylacetonitrile was dissolved in 250 ml of dry tetrahydrofuran and placed in a dry ice/isopropanol bath under N2. 69.0 ml of 1.6M n-butyl lithium (0.11 mole) was added dropwise over 30 minutes and the mixture stirred at -78° C. for one hour. The lithium salt of the nitrile precipitated as a yellow solid during this time. 71.0 g (0.50 mole) of methyl iodide was then added and stirring at -78° C. continued for an additional hour. The mixture was then poured into saturated ammonium chloride and the product extracted into diethyl ether, washed with saturated sodium chloride and dried over sodium sulfide. It was filtered and evaporated, redissolved in methylene chloride and passed through Florisel®. Evaporation gave 15.0 g of α-(p-methoxyphenyl)propionitrile as an orange oil.

WORKUP

后处理

  1. customplaced in a dry ice/isopropanol bath under N2
  2. customThe lithium salt of the nitrile precipitated as a yellow solid during this time
  3. stirringstirring at -78° C.
  4. waitcontinued for an additional hour
  5. extractionthe product extracted into diethyl ether
  6. washwashed with saturated sodium chloride
  7. dry with materialdried over sodium sulfide
  8. filtrationIt was filtered
  9. customevaporated
  10. dissolutionredissolved in methylene chloride
  11. customEvaporation