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
1.0 g of the compound obtained in Example 1 and 1 g of phenol were dissolved in 5 ml of benzene. Next, after dripping in a chilled mixed solution of 5 ml of benzene and 1 ml of pyridine, the solution was allowed to react for 4 hours at room temperature. After dripping in 50 ml of chilled 10% hydrochloric acid, the solution was extracted with benzene, water washed, and then dried with magnesium sulfate and reduced pressure concentrated. The remaining solid was subjected to chloroform mobile phase; silica gel column chromatography (2 cm ×60 cm) to prepare 2 ml fractions. These were then subjected to thin layer chromatography (silica gel, chloroform) and the fractions with an Rf range in the vicinity of 0.73 were collected. After reduced pressure condensation, the substance was recrystallized using n-hexane. The resulting 0.4 g of white needle shaped crystals had a melting point of between 120° to 121° C.
WORKUP
后处理
- customto react for 4 hours at room temperature
- extractionthe solution was extracted with benzene, water
- washwashed
- dry with materialdried with magnesium sulfate and reduced pressure
- concentrationconcentrated
- customsilica gel column chromatography (2 cm ×60 cm) to prepare 2 ml fractions
- customthe fractions with an Rf range in the vicinity of 0.73 were collected
- customAfter reduced pressure condensation
- customthe substance was recrystallized
- customof between 120° to 121° C.