Реакция #1135799
ord-32741cd822db46f59cef1825a0d38c2f
Уравнение реакции
Реактанты
Реагенты
Растворители
Условия реакции
Обработка
- 1Температураwith heating
- 2Температураunder reflux for one hour
- 3ДругоеAfter the reaction mixtures
- 4Температураwere cooled under ice-
- 5Температураcooling
- 6workup.ADDITIONwere added
- 7workup.STIRRINGthe resulting mixtures were stirred
- 8Температураwith heating
- 9Температураunder reflux for five hours
- 10ТемператураAfter cooling the mixtures
- 11workup.ADDITIONwas added
- 12Другоеthe reaction mixtures
- 13workup.STIRRINGwith stirring
- 14Экстракцияwere extracted with ethyl acetate
- 15СушкаThe organic layers were dried over anhydrous sodium sulfate
- 16Концентрированиеwere then concentrated under reduced pressure
Методика
A mixture of aluminium chloride 4.71 g, sodium azide 6.89 g and tetrahydrofuran 100 mL was stirred with heating under reflux for one hour. After the reaction mixtures were cooled under ice-cooling, thereto were added a mixture of the above-mentioned 1-chloro-3-isocyanato-2-methylbenzene and tetrahydrofuran 10 mL and the resulting mixtures were stirred with heating under reflux for five hours. After cooling the mixtures, to a mixture of sodium nitrite 10.59 g and water 300 mL was added the reaction mixtures with stirring. The mixtures were acidified with concentrated hydrochloric acid and were 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-chlorophenyl)-1,4-dihydrotetrazole-5-one.