Reacción #1594

ord-3ad3598473f04955b043e8d47bb746e6

Ecuación de reacción

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
Rendimiento 93.1%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathe mixture was heated at 60°-70° C. for 3 h
  2. 2
    TemperaturaThe resulting mixture was cooled
  3. 3
    FiltraciónThe resulting white solid was filtered
  4. 4
    Otrodried

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05726162uspto-grants-1998_03