Réaction #4440

ord-fa8318595eb54ee98aceafd5c8548e7b

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreA twelve-liter three neck flask fitted with an efficient mechanical stirrer
  2. 2
    workup.ADDITIONUpon completion of the addition the reaction mixture
  3. 3
    Températurewas cooled with an ice bath to 15° C.
  4. 4
    Autrethe product, which had precipitated
  5. 5
    Filtrationwas collected by filtration
  6. 6
    Lavagewashed with ether
  7. 7
    Autreair-dried

Mode opératoire

A twelve-liter three neck flask fitted with an efficient mechanical stirrer, 250 mL dropping funnel, and internal thermometer was charged with glacial acetic acid (5000 mL), pyridinium bromide perbromide (90%, 830 g, 2.60 mol) and 30% hydrobromic acid in acetic acid (525 mL). After stirring at room temperature for ninety minutes, 4-acetylpyridine (250 g, 2.07 mol) was added dropwise over forty-five minutes. Upon completion of the addition the reaction mixture was cooled with an ice bath to 15° C. and the product, which had precipitated, was collected by filtration, washed with ether and air-dried. The crude α-bromo-4-acetylpyridine hydrobromide (566.3 g, 97%) was sufficiently pure for subsequent reactions, mp. 177.5°-182.0° C.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US04725606uspto-grants-1988_02