Reacción #1135807
ord-c17ba9c97c674a27b8788e2bc5c14839
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1workup.STIRRINGthe resulting mixtures were stirred for fifteen minutes
- 2TemperaturaAfter cooling the mixtures
- 3workup.ADDITIONwas added the reaction solutions
- 4workup.STIRRINGwith stirring
- 5Extracciónwere extracted with ethyl acetate
- 6LavadoThe organic layers were washed with water and saturated saline
- 7Secadowere dried over anhydrous magnesium sulfate
- 8Concentraciónwere then concentrated under reduced pressure
Procedimiento
Under ice-cooling, to N,N-dimethylformamide 180 mL was added anhydrous aluminum chloride 16.0 g and the resulting mixtures were stirred for fifteen minutes. Thereto was added sodium azide 7.8 g and the resulting mixtures were stirred for fifteen minutes and thereto was then added 1-methoxy-3-isocyanato-2-methylbenzene 17.0 g and the resulting mixtures were heated at 80° C. for four and a half hours. After cooling the mixtures, to a mixture of sodium nitrite 25 g, water 2 L and ice 500 g was added the reaction solutions with stirring. The mixtures were acidified with 10% hydrochloric acid and were extracted with ethyl acetate. The organic layers were washed with water and saturated saline, and were dried over anhydrous magnesium sulfate and were then concentrated under reduced pressure to give 1-(2-methyl-3-methoxyphenyl)-1,4-dihydrotetrazole-5-one 16.2 g.