Реакция #1135803
ord-3165a9601fae418282e1ca16d1af2c12
Уравнение реакции
Реактанты
Реагенты
Растворители
Условия реакции
Обработка
- 1Температураwith heating
- 2Температураunder reflux for two hours
- 3ДругоеAfter the reaction mixtures
- 4Температураwere cooled under ice-
- 5Температураcooling
- 6workup.ADDITIONwas added
- 7workup.STIRRINGthe resulting mixtures were stirred
- 8Температураwith heating
- 9Температураunder reflux for ten hours
- 10ТемператураAfter cooling the mixtures
- 11workup.ADDITIONwas added
- 12Другоеthe reaction mixtures
- 13workup.STIRRINGwith stirring
- 14Экстракцияwere then 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 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.