Reaction #1135803
ord-3165a9601fae418282e1ca16d1af2c12
Reaction equation
Reactants
Reagents
Solvents
Conditions
Workup
- 1Temperaturewith heating
- 2Temperatureunder reflux for two hours
- 3OtherAfter the reaction mixtures
- 4Temperaturewere cooled under ice-
- 5Temperaturecooling
- 6workup.ADDITIONwas added
- 7workup.STIRRINGthe resulting mixtures were stirred
- 8Temperaturewith heating
- 9Temperatureunder reflux for ten hours
- 10TemperatureAfter cooling the mixtures
- 11workup.ADDITIONwas added
- 12Otherthe reaction mixtures
- 13workup.STIRRINGwith stirring
- 14Extractionwere then extracted with ethyl acetate
- 15DryingThe organic layers were dried over anhydrous sodium sulfate
- 16Concentrationwere then concentrated under reduced pressure
Procedure
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.