反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
A solution of 19.0 g. of 4-(4-acetyl-3-hydroxy-2-propylbenzyloxy)benzonitrile, 13.0 g. of sodium azide, and 10.9 g. of ammonium chloride in 250 ml. of dimethylformamide was heated to 115° C. for eight hours. An additional 13.0 g. of sodium azide and 10.9 g. of ammonium chloride were added every 2.5 hours during this period. The reaction was stirred overnight at room temperature and then heated an additional six hours with more reagents being added. The reaction mixture was then evaporated under reduced pressure and the residue was dissolved in 800 ml. of water. The solution was made acidic with hydrochloric acid and the resulting precipitate was filtered. The precipitate was dissolved in lN sodium hydroxide and the solution was washed once with ethyl acetate. The basic solution was made acidic with hydrochloric acid and the precipitate was recovered by filtration. The precipitate was crystallized first from isopropyl alcohol/ethyl acetate/water and then recrystallized from isopropyl alcohol providing 10.3 g. of the desired title product, m.p. 203°-205° C., IR, NMR.
WORKUP
后处理
- temperatureheated an additional six hours with more reagents
- additionbeing added
- customThe reaction mixture was then evaporated under reduced pressure
- dissolutionthe residue was dissolved in 800 ml
- filtrationthe resulting precipitate was filtered
- dissolutionThe precipitate was dissolved in lN sodium hydroxide
- washthe solution was washed once with ethyl acetate
- filtrationthe precipitate was recovered by filtration
- customThe precipitate was crystallized first from isopropyl alcohol/ethyl acetate/water
- customrecrystallized from isopropyl alcohol providing 10.3 g