Reacción #64082
ord-200ed0ecda1945e8b1b680337cb3c45e
Ecuación de reacción
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Extracciónfollowed by ether extraction
- 2SecadoThe ether phase was dried over anhydrous sodium sulfate and ether
- 3workup.DISTILLATIONwas distilled off
- 4workup.DISTILLATIONthe residue was subjected to distillation
Procedimiento
To 1.0 g of (2R, 5S, 6R)-2-trichloromethyl-5,6-dimethyl-1,3-dioxan-4-one obtained by procedure similar to Example 1-(4) were added 0.1 ml of concentrated sulfuric acid and 10 ml of 2-propanol, stirred at room temperature for one hour, and 20 ml of water was added followed by ether extraction. The ether phase was dried over anhydrous sodium sulfate and ether was distilled off, and then the residue was subjected to distillation to obtain 0.4 g of isopropyl (2S, 3R)-2-methyl-3-hydroxybutanoate. ##STR41##