Reaction #935

ord-f52f628e55bf48349560d5f7350120df

Reaction equation

O=C(OO)c1cccc(Cl)c1
m-chloroperbenzoic acid
O=S([O-])O.[Na+]
sodium bisulfite
COc1cccc(Sc2cccc(F)c2C#N)c1
2-fluoro-6-[(3-methoxyphenyl)thio]benzonitrile
COc1cccc(Sc2cccc(F)c2C#N)c1
2-Fluoro-6-[(3 -methoxyphenyl)thio]benzonitrile
O=C(OO)c1cccc(Cl)c1
m-chloroperbenzoic acid
COc1cccc(S(=O)c2cccc(F)c2C#N)c1
2-Fluoro-6-[(3-methoxyphenyl)sulfinyl]benzonitrile

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    ExtractionThe H2O solution was extracted with EtOAc
  2. 2
    DryingAfter drying over MgSO4 and solvent removal
  3. 3
    Otherthe resultant crude product was purified by flash column chromatography on silica gel with methylene chloride as the eluent
  4. 4
    OtherThis resulted in 1.7 g of 2-fluoro-6-[(3-methoxyphenyl)sulfinyl]benzonitrile as a solid

Procedure

To a solution of 2 g (7.7 mmol) of 2-fluoro-6-[(3-methoxyphenyl)thio]benzonitrile (Example 13) was added portionwise 1.6 g (9.3 mmol) of m-chloroperbenzoic acid. The resultant mixture was stirred for 24 h. Additional 0.16 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 eluent. This resulted in 1.7 g of 2-fluoro-6-[(3-methoxyphenyl)sulfinyl]benzonitrile as a solid: mp 103°-111° C.

Source

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