Réaction #893

ord-9053e57f398646fcad52b73dfd0e8b51

Équation de réaction

Cn1ncc(Br)c(Br)c1=O
4,5-Dibromo-2-methyl-3(2H)-pyridazinone
C[O-].[Na+]
sodium methoxide
COc1cnn(C)c(=O)c1Br
desired product
COc1cnn(C)c(=O)c1Br
4-Bromo-5-methoxy-2-methyl-3(2H)-pyridazinone

Conditions de réaction

Température
23°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe ice bath was removed
  2. 2
    AutreThe methanol was removed by evaporation at reduced pressure
  3. 3
    AutreThe residue was partitioned between dichloromethane and water
  4. 4
    SéchageThe organic layer was dried over magnesium sulfate
  5. 5
    Concentrationconcentrated

Mode opératoire

4,5-Dibromo-2-methyl-3(2H)-pyridazinone (20 g, Maybridge Chemical Company) was cooled in an ice bath and treated successively with methanol (200 mL) and sodium methoxide (12 mL of a 30% solution in methanol). The ice bath was removed and the reaction was allowed to stir at 23° C. for 3 h. The methanol was removed by evaporation at reduced pressure. The residue was partitioned between dichloromethane and water. The organic layer was dried over magnesium sulfate and concentrated to provide the desired product 17 g as a whim solid melting at 146°-147° C. 1 H NMR (CDCl3): 7.7 (1H), 4.0 (3H), 3.8 (3H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05723411uspto-grants-1998_03