反応 #1960493
ord-ebb990bc988347989bde908591a0fd3b
反応方程式
反応物
試薬
溶媒
反応条件
後処理
- 1workup.ADDITIONare added over the course of 30 min with ice-
- 2温度cooling
- 3抽出the mixture is extracted a number of times with MTBE
- 4洗浄The combined organic phases are washed with water and saturated sodium chloride solution
- 5その他the solution is dried
- 6その他after removal of the solvents
- 7その他is purified by column chromatography (SiO2, n-pentane:MTBE=2:1)
実験手順
8.0 g (31.2 mmol) of 7,8-difluoro-2-pentylchroman-6-ol are initially introduced in 75 ml of THF together with 6.75 g (37.4 mmol) of 1-(4-propylcyclohexyl)prop-2-yn-1-ol and 9.83 g (37.6 mmol) of triphenylphosphine, and 7.89 ml (40.6 mmol) of DIAD are added over the course of 30 min with ice-cooling. After 20 h at RT, semi-saturated sodium chloride solution is added, and the mixture is extracted a number of times with MTBE. The combined organic phases are washed with water and saturated sodium chloride solution, and the solution is dried using sodium sulfate. The residue remaining after removal of the solvents is purified by column chromatography (SiO2, n-pentane:MTBE=2:1), giving 7,8-difluoro-2-pentyl-6-[1-(4-propylcyclohexyl)prop-2-ynyloxy]chroman as a pale-brown oil.