Reaktion #2438517

ord-e302fca0861c4dc98d79193b3d42b186

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.WAITAfter the mixture was left
  2. 2
    Extraktionextracted
  3. 3
    TrocknenAfter the extract was dried over anhydrous magnesium sulfate, it
  4. 4
    Einengenwas concentrated under reduced pressure

Vorschrift

To the mixture of 4-chloro-6-o-fluoro phenyl-2-(6-metyl-2-pyridinyl)pyrimidine (1 g) was added sodium methoxide prepared from methanol (10 ml) and metallic sodium (0.1 g). After the mixture was left to stand at room temperature for 1 hour, water (30 ml) and ethyl acetate (100 ml) were added thereto, and then extracted. After the extract was dried over anhydrous magnesium sulfate, it was concentrated under reduced pressure to obtain 4-o-fluorophenyl-6-methoxy-2-(6-methyl-2-pyridinyl)pyrimidine (0.82 g).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04873248uspto-grants-1989_10