Réaction #554603

ord-bb47e8b728004f86b229dfa45cb49874

Équation de réaction

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

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurethe resulting mixture was refluxed overnight
  2. 2
    AutreThe organic layer was separated
  3. 3
    Extractionthe aqueous layer was extracted by 220 mL 2 dichloromethane
  4. 4
    Séchagedried over MgSO4
  5. 5
    AutreSolvent was then removed by rotary evaporator
  6. 6
    AutreThe crude product was purified by flash column chromatography with an eluent of hexane

Mode opératoire

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).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08623584B2uspto-grants-2014_01