Reaktion #1869164

Reaktionsgleichung

2-Amino-5-bromopyridine

2,5-hexanedione

p-toluenesulfonic acid

→

5-Bromo-2-(2,5-dimethylpyrrol-1-yl)pyridine

Ausbeute 80.0%

Lösungsmittel

heptane

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturrefluxed under Dean Stark conditions overnight
2. 2
   workup.DISTILLATIONThe equipment was set for distillation and heptane (18 L)
3. 3
   Sonstigewas removed by distillation
4. 4
   workup.ADDITIONSeed crystals were added
5. 5
   Sonstigeat 5° C.
6. 6
   Sonstigeovernight
7. 7
   FiltrationThe product was collected by filtration
8. 8
   Waschenwashed with heptane (2×6 L)
9. 9
   Sonstigedried at 45° C. under vacuum overnight

Vorschrift

2-Amino-5-bromopyridine (6.0 Kg, 34.7 mol), 2,5-hexanedione (4.35 Kg, 38.2 mol) and p-toluenesulfonic acid (12 g) were dissolved in heptane (36 L) and refluxed under Dean Stark conditions overnight. The equipment was set for distillation and heptane (18 L) was removed by distillation. The mixture was cooled to 20° C. for 60 minutes. Seed crystals were added and the mixture granulated at 20° C. for 2 hours and then at 5° C. overnight. The product was collected by filtration, washed with heptane (2×6 L) and dried at 45° C. under vacuum overnight. Yield=80% (7.0 Kg) δH (CDCl3 300 MHz) 2.20 (6H, s), 5.95 (2H, s), 7.15 (1H, d), 7.95 (1H, d), 8.70 (1H, s) ppm. MS m/z 253 (MH+, Br isotope).

Quelle