Reaktion #2207

ord-9050fa6258a9415bb85240ff78c07174

Reaktionsgleichung

O=C1CCC(c2ccc(Cl)cc2)=NN1
6-(4-chlorophenyl)-4,5-dihydropyridazinone
CC(=O)O
acetic acid
BrBr
bromine
O=c1ccc(-c2ccc(Cl)cc2)n[nH]1
6-(4-chlorophenyl)pyridazinone
Ausbeute 93.1%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe mixture was heated at 60°-70° C. for 3 h
  2. 2
    TemperaturThe resulting mixture was cooled
  3. 3
    FiltrationThe resulting white solid was filtered
  4. 4
    Sonstigedried

Vorschrift

To a solution of 6-(4-chlorophenyl)-4,5-dihydropyridazinone (11.75 g) and glacial acetic acid (100 ml) was added dropwise 3 ml of bromine and the mixture was heated at 60°-70° C. for 3 h. The resulting mixture was cooled and slowly poured into 400 ml of cold water. The resulting white solid was filtered and dried to yield 10.83 g (89%) of 6-(4-chlorophenyl)pyridazinone.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05728698uspto-grants-1998_03