反応 #64081
ord-4e34792d8ffc4b14a0fc392c6f7938d8
反応方程式
試薬
なし
溶媒
反応条件
詳細条件
See reaction.notes.procedure_details.
後処理
- 1抽出ether extraction
- 2乾燥After drying the ether phase over anhydrous sodium sulfate
- 3workup.DISTILLATIONthe ether was distilled off
- 4workup.DISTILLATIONthe residue was subjected to distillation
実験手順
To 1.0 g of (2R, 5R, 6R)-2-trichloromethyl-5,6-dimethyl-1,3-dioxan-4-one obtained by procedures similar to (1)-(4) of Example 1 were added 0.1 ml of concentrated sulfuric acid and 10 ml of 2-propanol and stirred at room temperature for one hour, and 20 ml of water was added to effect ether extraction. After drying the ether phase over anhydrous sodium sulfate, the ether was distilled off and the residue was subjected to distillation to give 0.4 g of isopropyl (2R, 3R)-2-methyl-3-hydroxybutanoate. The NMR chart is shown in FIG. 6. ##STR31##