Reaction #1869164

ord-1a09d052e34b42498da108bf302c1b78

Solvents

Conditions

Temperature
20°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Temperaturerefluxed under Dean Stark conditions overnight
  2. 2
    workup.DISTILLATIONThe equipment was set for distillation and heptane (18 L)
  3. 3
    Otherwas removed by distillation
  4. 4
    workup.ADDITIONSeed crystals were added
  5. 5
    Otherat 5° C.
  6. 6
    Otherovernight
  7. 7
    FiltrationThe product was collected by filtration
  8. 8
    Washwashed with heptane (2×6 L)
  9. 9
    Otherdried at 45° C. under vacuum overnight

Procedure

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).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07498329B2uspto-grants-2009_03