Réaction #927233

ord-464cfd84072745dd8aff821bf36140a1

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    SéchageThe ether layer was dried over magnesium sulfate
  2. 2
    Concentrationconcentrated under reduced pressure
  3. 3
    Autrethe resulting residue was purified by silica gel column chromatography (eluent; hexane-ethyl acetate mixed solvent)

Mode opératoire

To a solution of sodium hydride (60% oil, 2.55 g, 63.6 mol) in DMF (50 ml), trifluoroacetamide (8.99 g, 79.6 mmol) was added portionwise as about 10 portions with ice cooling. Subsequently, a solution of 6-iodo-1-hexyne (3.31 g, 15.9 mmol) in DMF (15 ml) was added to the reaction mixture. The reaction mixture was stirred at room temperature for four hours. The reaction mixture was added with saturated aqueous ammonium chloride (100 ml) and ether (100 ml) for extraction. The ether layer was dried over magnesium sulfate, and concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (eluent; hexane-ethyl acetate mixed solvent) to afford 2.0 g of 6-trifluoroacetamido-1-hexyne (yield; 65.4%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US06365350B1uspto-grants-2002_04