반응 #1929018

ord-f0477de3ac344b7dae102156f8d3826d

반응 방정식

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

반응 조건

온도
50°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타transferred under warm conditions to an erlenmeyer flask
  2. 2
    기타After 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
    여과The orange solid which then forms is filtered off
  7. 7
    세척washed with cold (0° C.) 95% ethanol
  8. 8
    기타After drying under vacuum at 40° C.
  9. 9
    기타(rotary evaporator)

실험 절차

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%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08945514B2uspto-grants-2015_02