Reaktion #1135796
ord-0cbabd7d0a7f4b7983de1f60ec35d596
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Temperaturwith heating
- 2Temperaturunder reflux for two hours
- 3SonstigeAfter the reaction mixtures
- 4Temperaturwere cooled under ice-
- 5Temperaturcooling
- 6workup.ADDITIONwas added
- 7workup.STIRRINGthe resulting mixtures were stirred
- 8Temperaturwith heating
- 9Temperaturunder reflux for ten hours
- 10TemperaturAfter cooling the mixtures
- 11workup.ADDITIONwas added
- 12Sonstigethe reaction mixtures
- 13workup.STIRRINGwith stirring
- 14Extraktionwere then extracted with ethyl acetate
- 15TrocknenThe organic layers were dried over anhydrous sodium sulfate
- 16Einengenwere then concentrated under reduced pressure
Vorschrift
A mixture of aluminium chloride 33.6 g, sodium azide 49.2 g and tetrahydrofuran 100 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-chloro-2-methylbenzoic acid chloride and tetrahydrofuran 100 mL and the resulting mixtures were stirred with heating under reflux for ten hours. After cooling the mixtures, to a mixture of sodium nitrite 75.6 g and water 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-chlorophenyl)-1.4-dihydrotetrazole-5-one.