Reacción #1885008
ord-2fbf3d2e27594174bd17be90650bd188
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Temperaturathe resulting mixture was refluxed overnight
- 2OtroThe organic layer was separated
- 3Extracciónthe aqueous layer was extracted by 220 mL 2 dichloromethane
- 4Secadodried over MgSO4
- 5OtroSolvent was then removed by rotary evaporator
- 6OtroThe crude product was purified by flash column chromatography with an eluent of hexane
Procedimiento
To a solution of benzo[b]thiophene-2-sulfonyl chloride (1.165 g, 5 mmol) in 25 mL of dichloromethane was added 3.6 mL of concentrated nitric acid (>22.05 mol/L) dropwise, the resulting mixture was refluxed overnight and cooled to room temperature before it was poured into 20 gram of crushed ice. The organic layer was separated and the aqueous layer was extracted by 220 mL 2 dichloromethane. The organic layers were combined and dried over MgSO4. Solvent was then removed by rotary evaporator. The crude product was purified by flash column chromatography with an eluent of hexane, followed by a gradient eluent of hexane/ethyl acetate (6/1-3/1) to afford 0.58 g of product (mixture of 65% of 4-nitro-benzo[b]thiophene-2-sulfonyl chloride and 35% of 7-nitro-benzo[b]thiophene-2-sulfonyl chloride).