Reacción #2267056

ord-110eed1e33904c0f82318c5594c14baa

Ecuación de reacción

O=S(=O)(O)O
sulfuric acid
CCC(C)(C)c1ccccc1
t-amylbenzene
[K+].[O-][I+2]([O-])[O-]
potassium iodate
CC(=O)OC(C)=O
acetic anhydride
CCC(C)(C)c1ccc([IH+])cc1.CCC(C)(C)c1ccc([IH+])cc1.O=S(=O)([O-])[O-]
(4-t-amylphenyl)iodonium sulfate

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaunder ice-cooling
  2. 2
    Temperaturacooling for 2 hours
  3. 3
    workup.STIRRINGthe mixture was stirred at room temperature for additional 10 hours
  4. 4
    Temperaturacooling
  5. 5
    Extracciónthe mixture was extracted with dichloromethane
  6. 6
    LavadoThe organic phase was washed with sodium hydrogencarbonate and water
  7. 7
    Concentraciónconcentrated

Procedimiento

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).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06887645B2uspto-grants-2005_05