Reaktion #1764265
ord-28ebeb9a1572473a8350aa05314ad2f0
Reaktionsgleichung
Edukte
Reagenzien
Reaktionsbedingungen
Aufarbeitung
- 1TemperaturUnder a nitrogen atmosphere and under ice-cooling
- 2workup.ADDITIONwere added
- 3Sonstigethe organic layer was partitioned
- 4WaschenThe organic layer was washed with brine
- 5Trocknendried with magnesium sulfate
- 6Sonstigethe solvent was removed under a vacuum
- 7workup.ADDITIONEthyl acetate (7 mL) and 4 N hydrochloric acid/ethyl acetate (20 mL) were added to the residue
- 8SonstigeThe solvent was removed under a vacuum, and ethyl acetate and sodium bicarbonate aqueous solution
- 9workup.ADDITIONwere added
- 10Sonstigethe organic layer was partitioned
- 11WaschenThe organic layer was washed with brine
- 12Trocknendried over anhydrous magnesium sulfate
- 13Sonstigethe solvent was removed under a vacuum
Vorschrift
Under a nitrogen atmosphere and under ice-cooling, methyl magnesium bromide (20.7 mL, 0.97 M tetrahydrofuran solution) was added dropwise into a tetrahydrofuran (60 mL) solution of (2R,5S)-5-(3,4-difluorophenyl)pyrrolidine-1,2-dicarboxylic acid 1-t-butyl ester 2-ethyl ester (2.5 g). After stirring for 2 hours at the same temperature, ammonium chloride aqueous solution and ethyl acetate were added, and the organic layer was partitioned. The organic layer was washed with brine and dried with magnesium sulfate, and the solvent was removed under a vacuum. Ethyl acetate (7 mL) and 4 N hydrochloric acid/ethyl acetate (20 mL) were added to the residue, and stirring was continued for 1 hour at room temperature. The solvent was removed under a vacuum, and ethyl acetate and sodium bicarbonate aqueous solution were added, and the organic layer was partitioned. The organic layer was washed with brine and dried over anhydrous magnesium sulfate, and the solvent was removed under a vacuum, and the title compound (1.66 g) was obtained. The physical property values are as follows.