反应 #1597038

ord-c22cce2bcd214c5d86aab9e7c6c65491

反应方程式

CCC(CC)CO
2-ethyl-1-butanol
C1CN2CCN1CC2
triethylenediamine
Cc1ccc(S(=O)(=O)Cl)cc1
p-toluenesulfonyl chloride
CCC(CC)COS(=O)(=O)c1ccc(C)cc1
title compound
收率 95.6%
CCC(CC)COS(=O)(=O)c1ccc(C)cc1
Toluene-4-sulfonic acid 2-ethylbutyl ester
收率 95.6%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    萃取extracted with 1.0N NaOH (2×40 mL)
  2. 2
    其他The organic layer was collected
  3. 3
    干燥dried over anhydrous sodium sulfate
  4. 4
    过滤filtered
  5. 5
    其他isolated by rotary evaporation

实验过程

To a solution of 2-ethyl-1-butanol (1.00 g, 9.79 mmol), triethylenediamine (1.32 g, 11.7 mmol) in DCM (30 mL, 0.5 mol) cooled to 0° C. was added p-toluenesulfonyl chloride (1.96 g, 10.3 mmol) in DCM (10 mL) The reaction mixture was stirred for 30 min, and extracted with 1.0N NaOH (2×40 mL). The organic layer was collected, dried over anhydrous sodium sulfate, filtered, and isolated by rotary evaporation to give the title compound (2.40 g).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08211894B2uspto-grants-2012_07