Reaktion #309129

ord-dac3bd636f5546449ef33bf3b694aa94

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturcooling
  2. 2
    ExtraktionThe resultant mixture was extracted with ethyl acetate
  3. 3
    TrocknenThe organic layer was dried over anhydrous magnesium sulfate
  4. 4
    Einengenconcentrated under reduced pressure

Vorschrift

Under a nitrogen stream, to a solution of [3-bromo-5-[(4-ethylphenyl)methyl]-naphthalen-2-yl]-methanol (326.2 mg, 0.92 mmol) and pyridinium p-toluenesulfonate (4.6 mg, 0.02 mmol) in THF (3.0 mL) was added 2-methoxypropene (0.44 mL, 4.6 mmol) under ice-cooling, and the resultant mixture was stirred at the same temperature for 1.5 hours. Saturated aqueous sodium hydrogen carbonate was added thereto. The resultant mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure, to thereby obtain the titled compound (393.2 mg, 100%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08207134B2uspto-grants-2012_06