Reaktion #2487282

ord-b21ef01d9d8549989270697b7b359ed0

Reaktionsgleichung

O=c1cc(-c2ccccc2)nc(-c2ccccc2)[nH]1
2,6-diphenyl-4(3H)-pyrimidinone
O=C1CCC(=O)N1Br
N-bromosuccinimide
O=c1[nH]c(-c2ccccc2)nc(-c2ccccc2)c1Br
5-bromo-2,6-diphenyl-4(3H)-pyrimidinone
Ausbeute 48.3%

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 100 g
  3. 3
    Sonstigecrushed ice and vacuum
  4. 4
    Filtrationfiltered
  5. 5
    Waschenwashing well with water
  6. 6
    Sonstigeair dried

Vorschrift

To a suspension of 13.37 g (56 mmol) of 2,6-diphenyl-4(3H)-pyrimidinone and 200 mL glacial acetic acid was added 15.1 g (84.8 mmol) of N-bromosuccinimide and the mixture was left to stir at room temperature for 60 h. The reaction was poured onto 100 g crushed ice and vacuum filtered, washing well with water, then air dried to yield 8.85 g (48%) 5-bromo-2,6-diphenyl-4(3H)-pyrimidinone, as a white solid. 1H-NMR (d6DMSO)δ7.55 (6H, m); 7.75 (2H, m); 8.15 (2H, m).

Quelle

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