Réaction #4440
ord-fa8318595eb54ee98aceafd5c8548e7b
Équation de réaction
Réactifs
Solvants
Conditions de réaction
Traitement
- 1AutreA twelve-liter three neck flask fitted with an efficient mechanical stirrer
- 2workup.ADDITIONUpon completion of the addition the reaction mixture
- 3Températurewas cooled with an ice bath to 15° C.
- 4Autrethe product, which had precipitated
- 5Filtrationwas collected by filtration
- 6Lavagewashed with ether
- 7Autreair-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.