Reacción #11332

ord-a974fa5d025a477aaee1506f61791129

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturacooled again
  2. 2
    workup.STIRRINGThe mixture was stirred for 30 minutes at room temperature
  3. 3
    Extracciónextracted with ethylacetate
  4. 4
    LavadoThe extract was washed with water
  5. 5
    Otrodried
  6. 6
    OtroThe solvent was evaporated
  7. 7
    LavadoThe obtained crystal was washed with hexane

Procedimiento

To a suspension of sodium hydride (60% in mineral oil, 2.4 g, 60 mmol) in DMF (100 ml) was added dropwise at an ice bath temperature a solution of pyrrole (3.35 g, 50 mmol) in DMF (5 ml). The mixture was stirred for 30 minutes at room temperature and cooled again. To the mixture was added dropwise a soluton of benzenesulfonylchloride (9.7 g, 5.5 mmol) in DMF (3 ml). The mixture was stirred for 30 minutes at room temperature and poured into ice-water, and extracted with ethylacetate. The extract was washed with water and dried. The solvent was evaporated. The obtained crystal was washed with hexane to give 1-benzenesulfonylpyrrole (8.4 g). Yield: 81%.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07098201B2uspto-grants-2006_08