反応 #1519100

反応方程式

THF

lithium aluminium hydride

THF

→

7-oxanorborn-2-en-5-ylmethanol

反応条件

後処理

1. 1
   その他quenched
2. 2
   workup.ADDITIONby cautiously adding an ice-water mixture
3. 3
   その他The organic phase was removed
4. 4
   抽出the aqueous phase extracted with ethyl acetate (3×200 ml)
5. 5
   洗浄The combined organic phases were washed with water (600 ml) and saturated sodium chloride solution (600 ml)
6. 6
   乾燥dried over sodium sulphate
7. 7
   濃縮concentrated under reduced pressure

実験手順

A solution of methyl 7-oxanorborn-2-en-5-ylcarbonate (16.163 g, 105 mmol, see Example 1) in THF (75 ml) was added dropwise with stirring and under nitrogen to a suspension of lithium aluminium hydride (4.376 g, 115 mmol) in anhydrous THF (100 ml), in such a way that the solution boiled gently. The reaction mixture was subsequently stirred at room temperature for another 12 h and then quenched by cautiously adding an ice-water mixture. The organic phase was removed and the aqueous phase extracted with ethyl acetate (3×200 ml). The combined organic phases were washed with water (600 ml) and saturated sodium chloride solution (600 ml), dried over sodium sulphate and concentrated under reduced pressure.

出典