HRID54590
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
3.1 g (10 mmol) of N-[3-methyl-2-(4-methyl-benzoyl)benzofuran-6-yl]-acetamide were suspended in 40 ml methanol. 20 ml 2.6 N HCl were added with stirring. The reaction mixture was heated to reflux. After 1 hour a clear solution was obtained. After 3 hours reflux the solution was cooled to room temperature and ethylacetate was added. The organic layer was washed once with NaOH-solution, two times with water, dried over Na4SO4 and concentrated in vacuo. The residue was further purified by crystallisation.
WORKUP
后处理
- temperatureThe reaction mixture was heated to reflux
- customAfter 1 hour a clear solution was obtained
- temperatureAfter 3 hours reflux the solution
- washThe organic layer was washed once with NaOH-solution, two times with water
- dry with materialdried over Na4SO4
- concentrationconcentrated in vacuo
- customThe residue was further purified by crystallisation