反应 #1925199
ord-90e01663831d40568edc0c1eca4743a4
反应方程式
反应条件
后处理
- 1其他A flask equipped with a stirrer
- 2温度under reflux for 6 hours
- 3过滤After the insolubles were filtered off
- 4workup.DISTILLATIONthe solvent was distilled off
- 5workup.ADDITIONethyl acetate was added to the resulting distillate, and the pH
- 6萃取ethyl acetate extraction
- 7萃取The resulting extract
- 8洗涤was washed with NaCl saturated water
- 9干燥dried over anhydrous sodium sulfate
- 10过滤filtered
- 11浓缩concentrated
- 12其他to thereby obtain 3.85 g of a crude product in the form of a yellowish brown solid
- 13其他The crude product was then purified by silica gel column chromatography
实验过程
A flask equipped with a stirrer and a thermometer was charged with 3.35 g (9.13 mmol) of 4-bromo-2-(trifluoromethoxy)iodobenzene and 19 ml of triethylamine under a nitrogen atmosphere. Then 1.48 g (9.13 mmol) of 2-[4-(3-methyl-3-hydroxybutyne-1-yl)phenoxy]ethanol, 13.7 mg (0.072 mmol) of copper (I) iodide, 63.2 mg (0.24 mmol) of triphenylphosphine, and 13.7 mg (0.020 mmol) of dichlorobis(triphenylphosphine)palladium were added at room temperature, and stirred under reflux for 6 hours. After the insolubles were filtered off and the solvent was distilled off, ethyl acetate was added to the resulting distillate, and the pH was adjusted to an acidity with 1N hydrochloric acid to effect ethyl acetate extraction. The resulting extract was washed with NaCl saturated water, dried over anhydrous sodium sulfate, filtered, and concentrated to thereby obtain 3.85 g of a crude product in the form of a yellowish brown solid. The crude product was then purified by silica gel column chromatography using hexane/ethyl acetate as an eluting solvent to obtain 3.0 g of 2-(4-{2-[4-bromo-2-(trifluoromethoxy)phenyl]ethynyl}phenoxy)ethanol in the form of a light yellow solid in a 82% yield.