Reaktion #169929

ord-e967a84eaca949648371400592c1fba9

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigePyridine and dichloromethane was evaporated in vacuo
  2. 2
    workup.ADDITIONWater (600 mL) was added
  3. 3
    ExtraktionThe reaction mixture was extracted with ethyl acetate (500 mL×3)
  4. 4
    Trocknenthe organic phase was dried over anhydrous sodium sulfate
  5. 5
    Filtrationfiltrated
  6. 6
    Einengenconcentrated
  7. 7
    Sonstigepurified by column chromatography (PE:EA=60:1)

Vorschrift

To a stirred suspension of 3-bromophenol (50 g, 0.29 mol) in pyridine (200 mL) and dichloromethane (100 mL) was added dropwise acetyl chloride (25 mL, 0.35 mol) at 0° C. and the mixture was stirred 18 h at room temperature. LC-MS showed that the reaction was complete. Pyridine and dichloromethane was evaporated in vacuo. Water (600 mL) was added and acidified with hydrochloric acid at pH 2. The reaction mixture was extracted with ethyl acetate (500 mL×3) and the organic phase was dried over anhydrous sodium sulfate, filtrated, concentrated and purified by column chromatography (PE:EA=60:1) to afford compound E-1 as a colorless liquid (46 g, 74%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08846736B2uspto-grants-2014_09