Реакция #933

ord-a610715a9a2049339b2b5008fb407eed

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ЭкстракцияThe H2O solution was extracted with EtOAc
  2. 2
    СушкаAfter drying over MgSO4 and solvent removal
  3. 3
    Другоеthe resultant crude product was purified by flash column chromatography on silica gel with methylene chloride as the fluent
  4. 4
    ДругоеThis resulted in 1.15 g of 2-fluoro-6-[(3-methoxyphenyl)sulfonyl]benzonitrile as a solid

Методика

To a solution of 2 g (7.7 mmol) of 2-fluoro-6-[(3-methoxyphenyl)thio]benzonitrile (Example 13) was added 2.93 g (17 mmol) of m-chloroperbenzoic acid. The resultant mixture was stirred for 24 h. Additional 0.29 g of m-chloroperbenzoic acid was added and the resultant mixture was stirred for 15 min. Excess sodium bisulfite was added, followed by water. The H2O solution was extracted with EtOAc. After drying over MgSO4 and solvent removal, the resultant crude product was purified by flash column chromatography on silica gel with methylene chloride as the fluent. This resulted in 1.15 g of 2-fluoro-6-[(3-methoxyphenyl)sulfonyl]benzonitrile as a solid: mp 113°-117° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05723452uspto-grants-1998_03