反応 #3012

ord-859a3ba4fca04957adca8f06dc6bef2a

反応方程式

[Br-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1
triphenylsulfonium bromide
Cc1ccc(S(=O)(=O)O)cc1
p-toluenesulfonic acid
Cc1ccc(S(=O)(=O)[O-])cc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
salt
収率 73.1%
Cc1ccc(S(=O)(=O)[O-])cc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Triphenylsulfonium Tosylate
収率 73.1%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度a gentle reflux for 15 hours under nitrogen
  2. 2
    抽出the clear solution was extracted with dichloromethane (4×75 ml)
  3. 3
    洗浄The combined organic extracts were washed with water until neutral (4×75 ml)
  4. 4
    乾燥dried (MgSO4 )
  5. 5
    その他The solvent was removed under reduced pressure
  6. 6
    その他the residue dried
  7. 7
    温度by heating at 80° C. in vacuo for 36 hours

実験手順

A solution of triphenylsulfonium bromide (6.87 g, 20.0 mmol) and p-toluenesulfonic acid (3.80 g, 20.0 mmol) in water (100 ml) was heated at a gentle reflux for 15 hours under nitrogen. After cooling to room temperature, the clear solution was extracted with dichloromethane (4×75 ml). The combined organic extracts were washed with water until neutral (4×75 ml) and dried (MgSO4 ). The solvent was removed under reduced pressure and the residue dried by heating at 80° C. in vacuo for 36 hours to give a crude onium salt as a off-white solid (6.35 g). Recrystallization from acetone-ethyl acetate gave triphenylsulfonium rosylate as a white crystalline solid (5.72 g, 66%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05731364uspto-grants-1998_03