Reacción #1135803
ord-3165a9601fae418282e1ca16d1af2c12
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Temperaturawith heating
- 2Temperaturaunder reflux for two hours
- 3OtroAfter the reaction mixtures
- 4Temperaturawere cooled under ice-
- 5Temperaturacooling
- 6workup.ADDITIONwas added
- 7workup.STIRRINGthe resulting mixtures were stirred
- 8Temperaturawith heating
- 9Temperaturaunder reflux for ten hours
- 10TemperaturaAfter cooling the mixtures
- 11workup.ADDITIONwas added
- 12Otrothe reaction mixtures
- 13workup.STIRRINGwith stirring
- 14Extracciónwere then extracted with ethyl acetate
- 15SecadoThe organic layers were dried over anhydrous sodium sulfate
- 16Concentraciónwere then concentrated under reduced pressure
Procedimiento
A mixture of aluminium chloride 181.0 g, sodium azide 265.0 g and tetrahydrofuran 30.0 mL was stirred with heating under reflux for two hours. After the reaction mixtures were cooled under ice-cooling, and thereto was added a mixture of the above-mentioned 3-bromo-2-methylbenzoic acid chloride and tetrahydrofuran 200 mL and the resulting mixtures were stirred with heating under reflux for ten hours. After cooling the mixtures, to a mixture of sodium nitrite 407 g and water 1,500 mL was added the reaction mixtures with stirring. The mixtures were acidified with concentrated hydrochloric acid and were then extracted with ethyl acetate. The organic layers were dried over anhydrous sodium sulfate and were then concentrated under reduced pressure to give 1-(2-methyl-3-bromophenyl)-1.4-dihydrotetrazole-5-one.