Reaktion #2487281

ord-a2589baa386f4cb68df2e82406942c40

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.WAITthe mixture was left
  2. 2
    workup.ADDITIONThe reaction was poured onto ice water and vacuum
  3. 3
    Filtrationfiltered
  4. 4
    Waschenwashing well with water
  5. 5
    SonstigeThe crude product was recrystallized from ethyl acetate

Vorschrift

To a solution of 1.0 g (3.94 mmol) of 2-phenyl-6-trifluoromethyl-4(3H)-pyrimidinone and 20 mL of glacial acetic acid was added 1.0 g (5.6 mmol) N-bromosuccinimide and the mixture was left to stir at room temperature for 16 h. The reaction was poured onto ice water and vacuum filtered, washing well with water. The crude product was recrystallized from ethyl acetate to yield 1.05 g (83.5%) of 5-bromo-2-phenyl-6-trifluoromethyl-4(3H)-pyrimidinone, as a white solid. 1H-NMR (d6DMSO)δ7.6 (3H, m); 8.15 (2H, m).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05453414uspto-grants-1995_09