Reacción #2161250
ord-23bc4e7f17454e83900db210da16f2fe
Ecuación de reacción
ethyl 4-nitro-1H-imidazole-2-carboxylate
cyclopropylmethyl bromide
potassium carbonate
→
Ethyl 1-(cyclopropylmethyl)-4-nitro-1H-imidazole-2-carboxylate
Reactivos
Ninguno
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1TemperaturaAfter cooling
- 2Extracciónextracted four times with ethyl acetate
- 3LavadoThe combined organic phases are washed once with water and three times with a saturated sodium chloride solution
- 4Secadodried with magnesium sulfate
- 5Concentraciónconcentrated in vacuo
- 6OtroThe crystalline residue is directly used further for the next reaction
Procedimiento
Under argon, 15 g (81 mmol) of ethyl 4-nitro-1H-imidazole-2-carboxylate are stirred with 13.13 g (97.2 mmol) of cyclopropylmethyl bromide and 22.4 g (162 mmol) of potassium carbonate in 165 ml of DMF at 80° C. for 1 h. After cooling, the reaction mixture is diluted with water and extracted four times with ethyl acetate. The combined organic phases are washed once with water and three times with a saturated sodium chloride solution, dried with magnesium sulfate and concentrated in vacuo. The crystalline residue is directly used further for the next reaction.