HRID2419928

反应详情

EQUATION

反应方程式

HRID 2419928 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

CONDITIONS

反应条件

温度
5 °C

PROCEDURE

实验过程

A solution of (±)-2-(2-naphthylmethoxy)-3,3,3-trifluoro-2-methylpropionyl chloride (4.3 g.) in benzene (20 ml.) is added, dropwise below 10° C., to a stirred solution of 3-pyridylmethanol (1.20 g.) and pyridine (1.10 g.) in benzene (20 ml.) and light petroleum (5 ml., b.p. 40°-60° C.). The mixture is stirred at 5° C. for 1 hour, and at ambient temperature for 18 hours. The mixture is filtered. The filtrate is diluted with ether, washed with water, aqueous sodium carbonate and water, dried with sodium sulphate, and evaporated to give an oil (4.1 g.). The oil is dissolved in a mixture of ethyl acetate, ethanol, and triethylamine (200:1:1) and is chromatographed on a column of silica gel (210 g.) made up in the same solvent. The column is eluted portionwise with the solvent. The first 350 ml. elutes an impurity (0.1 g.). The following 420 ml. of eluant is evaporated to give (±)-3-pyridylmethyl- 2-(2-naphtylmethoxy)-3,3,3-trifluoro-2-methylpropionate (3.9 g.) as a syrup.

WORKUP

后处理

  1. waitat ambient temperature for 18 hours
  2. filtrationThe mixture is filtered
  3. additionThe filtrate is diluted with ether
  4. washwashed with water, aqueous sodium carbonate and water
  5. dry with materialdried with sodium sulphate
  6. customevaporated
  7. customto give an oil (4.1 g.)
  8. customis chromatographed on a column of silica gel (210 g.)
  9. washThe column is eluted portionwise with the solvent
  10. customof eluant is evaporated