Reacción #1755455

ord-f73855ed2b2f431fbfae61338204e495

Ecuación de reacción

O=S(=O)(c1ccccc1)c1ccc(-n2cnc3ccccc32)cc1
1-(4′-phenylsulfonylphenyl)benzimidazole
C[O+](C)C.F[B-](F)(F)F
trimethyloxonium tetrafluoroborate
CCO
ethanol
Cn1c[n+](-c2ccc(S(=O)(=O)c3ccccc3)cc2)c2ccccc21.F[B-](F)(F)F
1-(4′-phenylsulfonylphenyl)-3-methylbenzimidazolium tetrafluoroborate
Rendimiento 80.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Filtraciónthe precipitate which forms is filtered off
  2. 2
    Lavadowashed with cold petroleum ether

Procedimiento

A solution of 1-(4′-phenylsulfonylphenyl)benzimidazole (6.7 g, 20 mmol) in dichloromethane (100 ml) is admixed at −10° C. with trimethyloxonium tetrafluoroborate (3.3 g, 22 mmol) and stirred under argon for 16 h. After adding ethanol, the precipitate which forms is filtered off and washed with cold petroleum ether. Yield: 80%.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07989091B2uspto-grants-2011_08