Reacción #8688

ord-aefda4e42cde42d1b7ffd52f52e1272a

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe organic solvent was evaporated
  2. 2
    workup.ADDITIONThe remaining suspension was diluted with water
  3. 3
    Extracciónextracted four times with EA
  4. 4
    Otroevaporated

Procedimiento

A solution of 2-phenylethanesulfonyl chloride (40.94 g) in THF (250 ml) was cooled to −20° C. before it was treated with sat. aq. ammonia (50 ml). The brown suspension was stirred at rt for 16 h. The mixture was neutralised with aq. HCl and the organic solvent was evaporated. The remaining suspension was diluted with water and extracted four times with EA. The organic layers were combined and evaporated to give 2-phenyl-ethanesulfonic acid amide (33.06 g) as orange solid. 1H-NMR(300 MHz, CDCl3): 3.15–3.21(m, 2H), 3.38–3.45(m, 2H), 4.59(s br, 2H), 7.21–7.37(m, 5H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07091201B2uspto-grants-2006_08