反応 #1135801
ord-d442d0aec58746beb02aa3cf9068cbe7
反応方程式
反応物
試薬
反応条件
後処理
- 1workup.STIRRINGthe resulting mixtures were stirred for fifteen minutes
- 2温度After cooling the mixtures
- 3workup.ADDITIONwas added the reaction solutions
- 4workup.STIRRINGwith stirring
- 5抽出were extracted with ethyl acetate
- 6洗浄The organic layers were washed with water and saturated saline
- 7乾燥were dried over anhydrous magnesium sulfate
- 8濃縮were then concentrated under reduced pressure
実験手順
Under ice-cooling, to N,N-dimethylformamide 220 mL was added anhydrous aluminum chloride 19.7 g and the resulting mixtures were stirred for fifteen minutes. Thereto was added sodium azide 9.6 g and the resulting mixtures were stirred for fifteen minutes and thereto was then added 1-bromo-3-isocyanato-2-methylbenzene 30.3 g and the resulting mixtures were heated at 80° C. for five hours. After cooling the mixtures, to a mixture of sodium nitrite 33 g, water 2 L and ice 500 g was added the reaction solutions with stirring. The mixtures were acidified with 10% hydrochloric acid and were extracted with ethyl acetate. The organic layers were washed with water and saturated saline, and were dried over anhydrous magnesium sulfate and were then concentrated under reduced pressure to give 1-(2-methyl-3-bromophenyl)-1,4-dihydrotetrazole-5-one 31.4 g.