Reacción #1106
ord-ed5d30e63cae482aa9ed8a44a63361f9
Ecuación de reacción
4-chloro-3-methoxy-2-methylpyridine
4-tert-butylaniline
NaOH
→
4-(4-tert-Butylanilino)-3-methoxy-2-methylpyridine
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1TemperaturaAfter cooling
- 2Extracciónthe product is extracted
- 3ConcentraciónAfter concentrating
- 4workup.DISTILLATIONthe excess of amine is distilled off in vacuo
- 5Otrothe residue is crystallized
Procedimiento
7.9 g of 4-chloro-3-methoxy-2-methylpyridine and 22.4 g of 4-tert-butylaniline are heated at 120° C. for 8 hours in 20 g of phenol. After cooling, the mixture is poured into NaOH and the product is extracted using methylene chloride. After concentrating, the excess of amine is distilled off in vacuo and the residue is crystallized using hexane. 9.5 g=55%