Reaktion #44611
ord-5751d1605b924848abd1cef897baba5b
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1workup.STIRRINGThis reaction solution was stirred under ice-
- 2Temperaturcooling for 1 hr
- 3workup.STIRRINGthis reaction solution was stirred at room temperature for 30 min
- 4SonstigeThe organic layer was separated
- 5Waschenwashed with saturated saline
- 6Trocknendried over anhydrous magnesium sulfate
- 7Einengenconcentrated under reduced pressure
- 8SonstigeThe obtained residue was purified by silica gel column chromatography (eluting solvent; heptane ethyl acetate=1:1)
Vorschrift
In nitrogen atmosphere, a THF solution (0.25 mL) of 1.06 M lithium tri-sec-butyl borohydride was dropwise added to a THF solution (3 mL) of (S)-4-[(1R,2R)-2-tert-butyldiphenylsilanyloxy-1-(3,4,5-trifluorophenyl)propyl]-6-methylmorpholin-2,3-dione (95 mg) at −20° C. This reaction solution was stirred at −20° C. for 30 min. To this reaction solution, a 5 N sodium hydroxide aqueous solution (0.03 mL) and a 30% hydrogen peroxide aqueous solution (0.07 mL) were added. This reaction solution was stirred under ice-cooling for 1 hr. A sodium hydrogensulfite powder (20 mg) was added to the reaction solution, and this reaction solution was stirred at room temperature for 30 min. To this reaction solution, saturated saline and ethyl acetate were added. The organic layer was separated, washed with saturated saline, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluting solvent; heptane ethyl acetate=1:1) to give 93 mg of the title compound. The physical property values of this compound were as follows: