Réaction #554603
ord-bb47e8b728004f86b229dfa45cb49874
Équation de réaction
Réactifs
Solvants
Conditions de réaction
Traitement
- 1Températurethe resulting mixture was refluxed overnight
- 2AutreThe organic layer was separated
- 3Extractionthe aqueous layer was extracted by 220 mL 2 dichloromethane
- 4Séchagedried over MgSO4
- 5AutreSolvent was then removed by rotary evaporator
- 6AutreThe 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).