반응 #1135804
ord-bd4264cf8f3e40eba55e56cea9e49663
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후처리
- 1온도with heating
- 2온도under reflux for two hours
- 3기타After the reaction mixtures
- 4온도were cooled under ice-
- 5온도cooling
- 6workup.ADDITIONwas added
- 7workup.STIRRINGthe resulting mixtures were stirred
- 8온도with heating
- 9온도under reflux for ten hours
- 10온도After cooling the mixtures
- 11workup.ADDITIONwas added
- 12기타the reaction mixtures
- 13workup.STIRRINGwith stirring
- 14추출were then extracted with ethyl acetate
- 15건조The organic layers were dried over anhydrous sodium sulfate
- 16농축were then concentrated under reduced pressure
실험 절차
A mixture of aluminium chloride 10.20 g, sodium azide 14.90 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-iodo-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 22.90 g and water 200 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-iodophenyl)-1.4-dihydrotetrazole-5-one.