反応 #9785
ord-e19001d0595c45359652e9e2aef71108
反応方程式
反応物
試薬
反応条件
後処理
- 1その他The solvent was evaporated
- 2乾燥The organic phase was dried over magnesium sulfate
- 3その他The product isolated
- 4その他after evaporation of the solvent
- 5その他was further purified by flash column chromatography
実験手順
A solution of {5-[4-(trifluoromethyl)phenyl]-3-furyl}methanol (0.15 g) in tetrahydrofuran (15 ml) stirred at 0° C. was treated with tributylphosphine (0.2 ml), as solution of ethyl(4-mercapto-2-methylphenoxy)acetate (0.150 g) in tetrahydrofuran (2 ml) and finally azodicarbonyldimorpholide (0.204 g). The reaction was allowed to warm to ambient temperature and stirred for 18 hours. The solvent was evaporated and the residue subjected to an aqueous work up using ethyl acetate and water. The organic phase was dried over magnesium sulfate. The product isolated after evaporation of the solvent was further purified by flash column chromatography using a cyclohexane:ethyl acetate (5:1) as eluent to give the title compound.