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 suspension of 3.36 g of sodium hydride (in mineral oil) in 50 ml of dimethylformamide is added dropwise at room temperature a solution of 15 g bis-(p-hydroxyphenyl)-methane in 50 ml dimethylformamide. The resulting solution is stirred at room temperature for one hour. Ten grams of benzyl chloride is added dropwise and the stirring is continued at room temperature overnight. After evaporation of the solvent under reduced pressure, the residue is treated with 100 ml of water and extracted twice with diethyl ether. The combined ether extracts are combined, dried over anhydrous magnesium sulfate, evaporated to dryness, and the resulting oil dissolved in hot ethanol. Bis(p-(benzyloxy)phenyl)methane crystallizes upon cooling and is collected by filtration. The mother liquors are evaporated to dryness and the crystalline mono-addition product is obtained by chromatography on silica gel with chloroform. After separation, the mono-benzyl ether is recrystallized from isopropyl ether, m.p. 95°-96°C.
WORKUP
后处理
- waitthe stirring is continued at room temperature overnight
- customAfter evaporation of the solvent under reduced pressure
- additionthe residue is treated with 100 ml of water
- extractionextracted twice with diethyl ether
- dry with materialdried over anhydrous magnesium sulfate
- customevaporated to dryness
- dissolutionthe resulting oil dissolved in hot ethanol
- customBis(p-(benzyloxy)phenyl)methane crystallizes
- temperatureupon cooling
- filtrationis collected by filtration
- customThe mother liquors are evaporated to dryness
- customthe crystalline mono-addition product is obtained by chromatography on silica gel with chloroform
- customAfter separation
- customthe mono-benzyl ether is recrystallized from isopropyl ether, m.p. 95°-96°C.