Реакция #938

ord-3a63765ce57f4be88697886cd8f75569

Уравнение реакции

O
water
O=S([O-])OO.[K+]
OXONE
Cc1cc(C)cc(Sc2cccc(F)c2C#N)c1
2-[(3,5-Dimethylphenyl)thio]-6-fluorobenzonitrile
O=S([O-])OO.[K+]
OXONE
Cc1cc(C)cc(S(=O)(=O)c2cccc(F)c2C#N)c1
2-[(3,5-dimethylphenyl)sulfonyl]-6-fluorobenzonitrile
Выход 65.0%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGAfter stirring 1 h
  2. 2
    workup.STIRRINGThe reaction was stirred for 18 h
  3. 3
    ДругоеThe solid was removed by vacuum filtration
  4. 4
    Промывкаwashed with 200 ml of methanol
  5. 5
    КонцентрированиеThe filtrate was concentrated to dryness
  6. 6
    Другоеchromatographed on silica gel (flash; Hex/EtOAc 1:1)

Методика

2-[(3,5-Dimethylphenyl)thio]-6-fluorobenzonitrile (Example 18) (1.0 g 3.9 mmol) was dissolved in 100 ml of methanol. A solution of OXONE®.dagger. (5.26 g, 8.6 mmol) in 30 ml of water was added dropwise with stirring. After stirring 1 h, another 1.5 equivalents of OXONE® (3.60 g 5.9 mmol) was added. The reaction was stirred for 18 h. The solid was removed by vacuum filtration and washed with 200 ml of methanol, then with 2×60 ml of acetone. The filtrate was concentrated to dryness and chromatographed on silica gel (flash; Hex/EtOAc 1:1) to provide 0.73 g (65%) of 2-[(3,5-dimethylphenyl)sulfonyl]-6-fluorobenzonitrile: mp 167°-168° C.

Источник

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