Reacción #2898

ord-ac7f5eb35ef547d1a557dea38319f19e

Ecuación de reacción

CI
iodomethane
Cc1n[nH]c(C)c1Br
4-Bromo-3,5-dimethylpyrazole
[H-].[Na+]
sodium hydride
O=C([O-])O.[Na+]
sodium hydrogen carbonate
[H][H]
hydrogen
Cc1nn(C)c(C)c1Br
title compound
Cc1nn(C)c(C)c1Br
4-Bromo-1,3,5-trimethylpyrazole

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwas added
  2. 2
    Otroevaporation under high vacuum
  3. 3
    Otrothe residue was purified by column chromatography

Procedimiento

4-Bromo-3,5-dimethylpyrazole (10 g) in dry dimethylformamide (50 ml) was added to a stirred suspension of sodium hydride (1.8 g) in dry dimethylformamide at 0° C. When the evolution of hydrogen was complete, iodomethane (8.9 g) was added dropwise. The mixture was allowed to warm to room temperature and after 30 minutes saturated aqueous sodium hydrogen carbonate (5 ml) was added. Following evaporation under high vacuum, the residue was purified by column chromatography to give the title compound.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05731335uspto-grants-1998_03