Reaktion #45372

ord-c82eff29b5eb41a6a8ee7e33a5e62a24

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationIt was filtered
  2. 2
    Einengenthe filtrate was concentrated
  3. 3
    workup.DISSOLUTIONThe residue was dissolved in methylene chloride
  4. 4
    Waschenwashed with 1 N sodium hydroxide
  5. 5
    Trocknendried over anhydrous sodium sulfate
  6. 6
    Filtrationfiltered
  7. 7
    Einengenconcentrated

Vorschrift

A mixture of silver sulfate (1.15 g, 3.68 mmol) and iodine (0.93 g, 3.68 mmol) were stirred in methanol at room temperature. A solution of p-ethylanisole (0.50 g, 3.68 mmol) in methanol was added dropwise to the stirring mixture. The mixture was stirred at room temperature until completion of the reaction. It was filtered and the filtrate was concentrated. The residue was dissolved in methylene chloride, washed with 1 N sodium hydroxide, dried over anhydrous sodium sulfate, filtered and concentrated. The title compound was obtained without further purification. 1H NMR (CDCl3, 500 MHz) δ 7.64 (d, J=2.0 Hz, 1H), 7.15 (dd, J=8.5, 2.0 Hz, 1H), 6.77 (d, J=8.0 Hz, 1H), 3.88 (s, 3H), 2.58 (q, J=15.5, 8.0 Hz, 2H), 1.23 (t, J=7.5 Hz, 3H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07737295B2uspto-grants-2010_06