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 stirred mixture of diethyl acetamidomalonate (217 g, 1.0 mol) and 2,3-dibromopropene (240 g, 1.2 mol) in dry tetrahydrofuran (2.50 L), under nitrogen, was added sodium hydride (26.4 g, 1.1 mol) in several portions. The reaction mixture was stirred at room temperature for 30 min, then heated to reflux. After heating for 18 h, the resultant slurry was cooled to room temperature and suction filtered through a short pad of silica gel. The solid residue was washed with tetrahydrofuran (2×50 mL), and the filtrates were combined and concentrated. The residue was dissolved in ethyl acetate (2.0 L), washed with water and brine, and then was dried over MgSO4. Filtration and concentration gave a yellow oil which solidified upon drying. The resultant solid was recrystallized from a mixture of hot ethyl acetate/hexane to give 301 g (89%) of the desired product: m.p. 85°-87° C.
WORKUP
后处理
- temperatureheated to reflux
- temperatureAfter heating for 18 h
- temperaturethe resultant slurry was cooled to room temperature
- filtrationsuction filtered through a short pad of silica gel
- washThe solid residue was washed with tetrahydrofuran (2×50 mL)
- concentrationconcentrated
- dissolutionThe residue was dissolved in ethyl acetate (2.0 L)
- washwashed with water and brine
- dry with materialwas dried over MgSO4
- filtrationFiltration and concentration
- customgave a yellow oil which
- customupon drying
- customThe resultant solid was recrystallized from a mixture of hot ethyl acetate/hexane