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
To a solution of diethyl malonate (11.0 g) in tetrahydrofuran (60 ml) was gradually added sodium hydride (60%, oil, 2.50 g) at 0° C. The mixture was stirred for 10 min and a solution of 4-chloromethyl-5-(4-methylphenyl)isoxazole (6.48 g) in tetrahydrofuran (80 ml) was added dropwise at 0° C. The mixture was stirred at room temperature for 15 hr. The reaction mixture was poured into 2N hydrochloric acid and the mixture was extracted with ethyl acetate. The ethyl acetate layer was concentrated and the residue was dissolved in a mixture of 6N hydrochloric acid (80 ml) and acetic acid (120 ml). The mixture was heated under reflux for 8 hr. The reaction mixture was concentrated, and water was added to the residue. The obtained colorless crystals were filtrated, dried and recrystallized from ethyl acetate-hexane to give a colorless prism (5.03 g, yield 70%) of 3-[5-(4-methylphenyl)-4-isoxazolyl]propionic acid. melting point: 121–122° C.
WORKUP
后处理
- customat 0° C
- stirringThe mixture was stirred at room temperature for 15 hr
- extractionthe mixture was extracted with ethyl acetate
- concentrationThe ethyl acetate layer was concentrated
- dissolutionthe residue was dissolved in a mixture of 6N hydrochloric acid (80 ml) and acetic acid (120 ml)
- temperatureThe mixture was heated
- temperatureunder reflux for 8 hr
- concentrationThe reaction mixture was concentrated
- additionwater was added to the residue
- filtrationThe obtained colorless crystals were filtrated
- customdried
- customrecrystallized from ethyl acetate-hexane