Reacción #1885008

ord-2fbf3d2e27594174bd17be90650bd188

Ecuación de reacción

O=S(=O)(Cl)c1cc2ccccc2s1
benzo[b]thiophene-2-sulfonyl chloride
O=[N+]([O-])O
nitric acid
O=[N+]([O-])c1c(S(=O)(=O)Cl)sc2ccccc12
product
O=[N+]([O-])c1c(S(=O)(=O)Cl)sc2ccccc12
mono nitro-benzo[b]thiophene-2-sulfonyl chloride

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathe resulting mixture was refluxed overnight
  2. 2
    OtroThe organic layer was separated
  3. 3
    Extracciónthe aqueous layer was extracted by 220 mL 2 dichloromethane
  4. 4
    Secadodried over MgSO4
  5. 5
    OtroSolvent was then removed by rotary evaporator
  6. 6
    OtroThe 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).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08343706B2uspto-grants-2013_01