Reacción #2021475

ord-cb9cd00415714cfdadc5e0a42fc263c9

Ecuación de reacción

O=S(c1ccccc1)c1ccccc1
diphenylsulfoxide
Cc1ccccc1
toluene
O=C(OC(=O)C(F)(F)F)C(F)(F)F
trifluoroacetic anhydride
O=S(=O)(O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F
perfluorobutanesulfonic acid
Cc1ccc([S+](c2ccccc2)c2ccccc2)cc1.O=S(=O)([O-])C(F)(F)C(F)(F)C(F)(F)C(F)(F)F
4-methylphenyldiphenylsulfonium perfluorobutanesulfonate

Condiciones de reacción

Temperatura
2°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Concentraciónthe lower layer was concentrated
  2. 2
    workup.ADDITIONdiluted with 100 parts of chloroform
  3. 3
    LavadoThe obtained chloroform solution was washed 11 times with 50 parts of ion-exchange water
  4. 4
    Concentraciónconcentrated

Procedimiento

Into a four-necked flask were charged 5.06 parts of diphenylsulfoxide and 50.6 parts of toluene, and the mixture was cooled to 2° C. Then, 10.5 parts of trifluoroacetic anhydride and 7.50 parts of perfluorobutanesulfonic acid were added and the mixture was stirred at the same temperature for 60 minutes. After standing, the lower layer was concentrated and diluted with 100 parts of chloroform. The obtained chloroform solution was washed 11 times with 50 parts of ion-exchange water and concentrated to give 12.0 parts of 4-methylphenyldiphenylsulfonium perfluorobutanesulfonate, which is referred to herein as PAG4.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06383713B1uspto-grants-2002_05