Reacción #956412
ord-a78fc81410f045249dfdb20a289d0faf
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Temperatura
50°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1workup.ADDITIONwas added
- 2OtroAfter the reaction liquid
- 3Temperaturawas cooled
- 4Otrothe reaction liquid
- 5Extracciónwas extracted with chloroform
- 6SecadoAfter the organic layer was dried over anhydrous sodium sulfate
- 7workup.DISTILLATIONthe solvent was distilled off under reduced pressure
Procedimiento
To a mixture of 1-(isopropylsulfanyl)-4-methyl-2-nitrobenzene (Preparation Example 287) (6.60 g) and chloroform (150 mL), m-chloroperbenzoic acid (18.0 g) was added and stirred at 50° C. for 12 hours. After the reaction liquid was cooled, saturated aqueous sodium hydrogen carbonate and 5% aqueous sodium sulfite were added, and the reaction liquid was extracted with chloroform. After the organic layer was dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure to give 2-(isopropylsulfonyl)-4-methyl-1-nitrobenzene (7.41 g) as a yellow solid.