Réaction #6818

ord-681f0d0de09a4023ad7560518cc95756

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe volatile material are evaporated by a rotary evaporator
  2. 2
    workup.DISSOLUTIONthe resulting residue was dissolved in 50 mL dichloromethane
  3. 3
    Lavagewashed with 1 M HCl (50 mL)
  4. 4
    SéchageThe dichloromethane layer was dried over sodium sulfate
  5. 5
    Autreevaporated to dryness under vacuum
  6. 6
    AutreThe residue was purified by column chromatography (ethyl acetate/dichloromethane)

Mode opératoire

A solution of pent-4-ynoic acid (1.0 g, 10 mmol), iodobenzene (2.3 ml, 20 mmol), copper(I) iodide (75 mg, 0.40 mmol) and dichlorobis(triphenylphosphine)-platinum(II) (140 mg, 0.20 mmol) in 20 mL of diethylamine was stirred at rt for 3 days. The volatile material are evaporated by a rotary evaporator and the resulting residue was dissolved in 50 mL dichloromethane and washed with 1 M HCl (50 mL). The dichloromethane layer was dried over sodium sulfate and evaporated to dryness under vacuum. The residue was purified by column chromatography (ethyl acetate/dichloromethane) to afford 5-phenylpent-4-ynoic acid (0.49 g).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07084154B2uspto-grants-2006_08