反応 #1135803
ord-3165a9601fae418282e1ca16d1af2c12
反応方程式
反応物
試薬
溶媒
反応条件
後処理
- 1温度with heating
- 2温度under reflux for two hours
- 3その他After the reaction mixtures
- 4温度were cooled under ice-
- 5温度cooling
- 6workup.ADDITIONwas added
- 7workup.STIRRINGthe resulting mixtures were stirred
- 8温度with heating
- 9温度under reflux for ten hours
- 10温度After cooling the mixtures
- 11workup.ADDITIONwas added
- 12その他the reaction mixtures
- 13workup.STIRRINGwith stirring
- 14抽出were then extracted with ethyl acetate
- 15乾燥The organic layers were dried over anhydrous sodium sulfate
- 16濃縮were then concentrated under reduced pressure
実験手順
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.