反応 #1063362

ord-8a1496379aea4c7c9c64f669c0b49a23

反応方程式

Cc1ccc(S(=O)(=O)Cl)cc1
p-toluenesulfonyl chloride
NCCCNCCCN
1,5,9-triazanonane
Cc1ccc(S(=O)(=O)NCCCN(CCCNS(=O)(=O)c2ccc(C)cc2)S(=O)(=O)c2ccc(C)cc2)cc1
crude product
収率 59.0%
Cc1ccc(S(=O)(=O)NCCCN(CCCNS(=O)(=O)c2ccc(C)cc2)S(=O)(=O)c2ccc(C)cc2)cc1
1,5,9-Tris(p-toluenesulfonyl)-1,5,9-triazanonane
収率 59.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度maintaining the temperature ≤60° C
  2. 2
    workup.ADDITIONThe addition required 15 minutes
  3. 3
    その他The solvent was removed in vacuo
  4. 4
    workup.DISSOLUTIONthe resulting yellow oil was dissolved in ethyl acetate (1 l)
  5. 5
    その他The ethyl acetate layer was separated
  6. 6
    洗浄washed with 0.1N HCl, H2O and saturated NaCl solution
  7. 7
    乾燥dried (MgSO4)
  8. 8
    その他the solvent was removed in vacuo

実験手順

To a stirred solution of p-toluenesulfonyl chloride (240 g, 1.26 mole) in pyridine (600 ml) at 0° C. was added a solution of 1,5,9-triazanonane (50.0 g, 0.381 mole) in pyridine (100 ml) under a dry nitrogen atmosphere, maintaining the temperature ≤60° C. The addition required 15 minutes. The solvent was removed in vacuo and the resulting yellow oil was dissolved in ethyl acetate (1 l) and H2O (500 ml). The ethyl acetate layer was separated, washed with 0.1N HCl, H2O and saturated NaCl solution and dried (MgSO4). The solution was decolorized with silica gel and the solvent was removed in vacuo to give 133 g (59% yield) of the crude product as a glassy solid: 1H NMR (CDCl3) δ1.71 (quint, J=6.6 Hz, 4 H), 2.42 (s, 6 H), 2.43 (s, 3 H), 2.96 (quart, J=6.4 Hz, 4 H), 3.11 (t, J=6.8 Hz, 4 H), 5.12 (t, J=6.6 Hz, 2 H), 7.30 (m, 6 H), 7.63 (m, 2 H), 7.73 (m, 4 H).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05610293uspto-grants-1997_03