反应 #1929018

ord-f0477de3ac344b7dae102156f8d3826d

反应方程式

O
water
NCCNCCN
diethylenetriamine
Cc1ccc(S(=O)(=O)Cl)cc1
p-toluenesulfonyl chloride
Cc1ccc(S(=O)(=O)C(CNCCN)N(S(=O)(=O)c2ccc(C)cc2)S(=O)(=O)c2ccc(C)cc2)cc1
desired product
Cc1ccc(S(=O)(=O)C(CNCCN)N(S(=O)(=O)c2ccc(C)cc2)S(=O)(=O)c2ccc(C)cc2)cc1
tris(p-toluenesulfonyl)diethylenetriamine

反应条件

温度
50°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他transferred under warm conditions to an erlenmeyer flask
  2. 2
    其他After returning to ambient temperature
  3. 3
    workup.WAITThe mixture is left
  4. 4
    workup.STIRRINGstirring overnight at ambient temperature
  5. 5
    workup.WAITis then placed in an ice bath for 2 hours
  6. 6
    过滤The orange solid which then forms is filtered off
  7. 7
    洗涤washed with cold (0° C.) 95% ethanol
  8. 8
    其他After drying under vacuum at 40° C.
  9. 9
    其他(rotary evaporator)

实验过程

115 g (0.6 mol) of p-toluenesulfonyl chloride are dissolved in 250 ml of pyridine at ambient temperature. A solution of diethylenetriamine (21.5 ml, 0.2 mol) in pyridine (30 ml) is added dropwise. The reaction mixture is stirred at 50° C. for 90 minutes and then transferred under warm conditions to an erlenmeyer flask. After returning to ambient temperature, 200 ml of water are added. The mixture is left stirring overnight at ambient temperature and is then placed in an ice bath for 2 hours. The orange solid which then forms is filtered off and washed with cold (0° C.) 95% ethanol. After drying under vacuum at 40° C. (rotary evaporator), the desired product is obtained in the form of a light yellow solid (92 g, yield 81%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08945514B2uspto-grants-2015_02