Reacción #696714
ord-ca770469cfe8464d962e399650e6a123
Ecuación de reacción
Ethyl 1-methylimidazole-2-carboxylate
nitric acid
→
Ethyl 1-methyl-4-nitroimidazole-2-carboxylate
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Temperaturamaintaining a temperature of 0° C
- 2TemperaturaThe reaction was then refluxed with an efficient condenser (-20° C.) in a well ventilated hood for 50 min
- 3TemperaturaThe reaction was cooled with an ice bath
- 4Otroquenched
- 5workup.ADDITIONby pouring onto 10 L ice
- 6ExtracciónThe resulting blue solution was then extracted with 20 L DCM
- 7Secadothe combined extracts dried (sodium sulfate)
- 8Concentraciónconcentrated in vacuo
- 9Otroto yield a tan solid which
- 10Otrowas recrystallized from 22 L of 21:1 carbon tetrachloride/ethanol
- 11FiltraciónThe resulting white crystals are collected by vacuum filtration
Procedimiento
Ethyl 1-methylimidazole-2-carboxylate was carefully dissolved in 1000 mL of concentrated sulfuric acid cooled to 0° C. 90% nitric acid (1 L) was slowly added maintaining a temperature of 0° C. The reaction was then refluxed with an efficient condenser (-20° C.) in a well ventilated hood for 50 min. The reaction was cooled with an ice bath, and quenched by pouring onto 10 L ice. The resulting blue solution was then extracted with 20 L DCM, the combined extracts dried (sodium sulfate) and concentrated in vacuo to yield a tan solid which was recrystallized from 22 L of 21:1 carbon tetrachloride/ethanol. The resulting white crystals are collected by vacuum filtration.