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 solution of 5.0 grams (0.029 mole) of 2-fluoroethyl 4-hydroxymethylphenyl ether in 50 ml of tetrahydrofuran was added 15 ml of a 50% aqueous, sodium hydroxide solution, 7.6 grams (0.060 mole) of 1-bromo-2-fluoroethane, and 0.78 gram (0.0023 mole) of tetrabutylammonium hydrogen sulfate. The resultant mixture was stirred and heated at reflux for approximately 18 hours. The mixture was cooled and was extracted with diethyl ether. The extract was washed in succession with a dilute, aqueous, sodium hydroxide solution, an aqueous 10% lithium chloride solution, and a saturated, aqueous, sodium chloride solution. The washed organic phase was dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure to leave an oil. Analysis of this oil by nmr indicated a large amount of starting material remained. The oil was again heated at reflux with the same quantities of the above reactants for 30 minutes. The reaction mixture was cooled and extracted with diethyl ether. The extract was washed several times with water followed by an aqueous, 15% lithium chloride solution. The washed extract was dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure leaving an oil. Analysis of this oil by nmr indicated starting material was still present. This oil was heated at reflux with the same quantities of the above reagents for approximately 24 hours. The mixture was cooled and extracted with diethyl ether. The extract was washed with water and was dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure to yield 1.9 grams of 4-(2-fluoroethoxymethyl)phenyl 2-fluoroethyl ether as an oil.
WORKUP
后处理
- temperatureheated
- temperatureat reflux for approximately 18 hours
- temperatureThe mixture was cooled
- extractionwas extracted with diethyl ether
- washThe extract was washed in succession with a dilute
- dry with materialThe washed organic phase was dried over anhydrous magnesium sulfate
- filtrationfiltered
- customThe filtrate was evaporated under reduced pressure
- customto leave an oil
- temperatureThe oil was again heated
- temperatureat reflux with the same quantities of the above reactants for 30 minutes
- temperatureThe reaction mixture was cooled
- extractionextracted with diethyl ether
- washThe extract was washed several times with water
- extractionThe washed extract
- dry with materialwas dried over anhydrous magnesium sulfate
- filtrationfiltered
- customThe filtrate was evaporated under reduced pressure
- customleaving an oil
- temperatureThis oil was heated
- temperatureat reflux with the same quantities of the above reagents for approximately 24 hours
- temperatureThe mixture was cooled
- extractionextracted with diethyl ether
- washThe extract was washed with water
- dry with materialwas dried over anhydrous magnesium sulfate
- filtrationfiltered
- customThe filtrate was evaporated under reduced pressure