反应 #1166459

ord-54fa65e2709b496fb61caff34a76b847

反应方程式

Cl
hydrochloric acid
Cc1ccc(S(=O)(=O)Cl)cc1
p-toluenesulfonic acid chloride
CCCCCOC(C)CCCCCO
6-pentyloxyheptanol
O
water
CCCCCOC(C)CCCCCOS(=O)(=O)c1ccc(C)cc1
(6-pentyloxyheptyl)-p-toluenesulfonate
收率 82.9%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    萃取was extracted with ethyl acetate
  2. 2
    洗涤The resultant solution was washed with water
  3. 3
    干燥dried with anhydrous magnesium sulfate

实验过程

A solution of 2.26 g of p-toluenesulfonic acid chloride in 5 ml of pyridine was gradually added dropwise to a cooled solution of 2.04 g of 6-pentyloxyheptanol in 8 ml of pyridine for 7 min. below 5° C. After stirring for 5 hours at room temperature, the reaction mixture was injected into 150 ml of cold water and, after being acidified to pH 3 with 6N-hydrochloric acid, was extracted with ethyl acetate. The resultant solution was washed with water and dried with anhydrous magnesium sulfate, followed by distilling-off of the solvent to obtain 2.98 g of (6-pentyloxyheptyl)-p-toluenesulfonate.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05580489uspto-grants-1996_12