反応 #1755455

ord-f73855ed2b2f431fbfae61338204e495

反応方程式

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
収率 80.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過the precipitate which forms is filtered off
  2. 2
    洗浄washed with cold petroleum ether

実験手順

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%.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07989091B2uspto-grants-2011_08