反应 #1755455

ord-f73855ed2b2f431fbfae61338204e495

反应方程式

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
收率 80.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤the precipitate which forms is filtered off
  2. 2
    洗涤washed with cold petroleum ether

实验过程

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%.

来源

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