Reaktion #937

ord-6ddfb59c25f34fe781aa3d4f78fc3efa

Reaktionsgleichung

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)c2cccc(F)c2C#N)c1
2-[(3,5-dimethylphenyl)sulfinyl]-6-fluorobenzonitrile
Ausbeute 47.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGAfter stirring 1.5 h
  2. 2
    Sonstigethe solid was removed by vacuum filtration
  3. 3
    Waschenwashed with 3×50 ml of methanol
  4. 4
    EinengenThe filtrate was concentrated to dryness
  5. 5
    Sonstigechromatographed on silica
  6. 6
    Sonstigeget (flash; Hex/EtOAc 2:1)

Vorschrift

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. (2.63 g, 4.3 mmol) in 15 ml of water was added dropwise with stirring. After stirring 1.5 h, the solid was removed by vacuum filtration and washed with 3×50 ml of methanol. The filtrate was concentrated to dryness and chromatographed on silica get (flash; Hex/EtOAc 2:1) to provide 0.5 g (47%) of 2-[(3,5-dimethylphenyl)sulfinyl]-6-fluorobenzonitrile: mp 146°-147° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05723452uspto-grants-1998_03