HRID905053

反应详情

EQUATION

反应方程式

HRID 905053 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

3 g of 2-tosyloxymethyl-3,4-dihydro-2H-pyran and 1.91 g of p-chlorobenzyl alcohol were dissolved in 40 ml of diethyl ether, and 2-3 drops of phosphorus oxytrichloride were added to the resulting solution. The mixture was then allowed to react at room temperature for 1.5 days, after which 2 drops of triethylamine were added and the mixture was concentrated by evaporation under reduced pressure. The residue was subjected to column chromatography through silica gel, eluted with a 8:1 by volume mixture of hexane and ethyl acetate, to give 3.44 g of trans-6-(4-chlorobenzyloxy)-2-tosyloxymethyltetrahydropyran (having the lesser polarity), 0.59 g of cis-6-(4-chlorobenzyloxy)-2-tosyloxymethyltetrahydropyran (having the greater polarity) and 0.86 g of an approximately 1:1 cis/trans mixture.

WORKUP

后处理

  1. customto react at room temperature for 1.5 days
  2. concentrationthe mixture was concentrated by evaporation under reduced pressure
  3. washeluted with a 8:1 by volume mixture of hexane and ethyl acetate