反応 #2267057

ord-806f0db4e285436185823604d705889d

反応方程式

CCC(C)(C)c1ccc([IH+])cc1.CCC(C)(C)c1ccc([IH+])cc1.O=S(=O)([O-])[O-]
sulfate
CCC(C)(C)c1ccc([IH+])cc1.CCC(C)(C)c1ccc([IH+])cc1.O=S(=O)([O-])[O-]
(4-t-amylphenyl)iodonium sulfate
C[N+](C)(C)C.O=S(=O)([O-])c1c(F)c(F)c(F)c(F)c1F
tetramethylammonium pentafluorobenzenesulfonate
CCC(C)(C)c1ccc([I+]c2ccc(C(C)(C)CC)cc2)cc1.O=S(=O)([O-])c1c(F)c(F)c(F)c(F)c1F
di(4-t-amylphenyl)iodonium pentafluorobenzenesulfonate

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    抽出the solution was extracted with dichloromethane
  2. 2
    洗浄Then the organic phase was washed with a 5% aqueous solution of tetramethylammonium hydroxide and water
  3. 3
    濃縮concentrated

実験手順

60 g of t-amylbenzene, 39.5 g of potassium iodate, 81 g of acetic anhydride and 170 ml of dichloromethane were mixed together. Then 66.8 g of conc. sulfuric acid was slowly added dropwise thereinto under ice-cooling. After stirring under ice-cooling for 2 hours, the mixture was stirred at room temperature for additional 10 hours. 500 ml of water was added to the liquid reaction mixture under ice-cooling and the mixture was extracted with dichloromethane. The organic phase was washed with sodium hydrogencarbonate and water and then concentrated to give (4-t-amylphenyl)iodonium sulfate. This sulfate was added to a solution of tetramethylammonium pentafluorobenzenesulfonate in excess. After adding 500 ml of water, the solution was extracted with dichloromethane. Then the organic phase was washed with a 5% aqueous solution of tetramethylammonium hydroxide and water and then concentrated to give di(4-t-amylphenyl)iodonium pentafluorobenzenesulfonate (III-1).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06887645B2uspto-grants-2005_05