反应详情

To a solution of 1-(4(S)-benzyl-2,2-dimethyl-oxazolidin-3-yl)-2-[1-(biphenyl-4-yl)1H-pyrrol-3-yl]-2-hydroxy-ethanone (867 mg, 1.86 mmol) in dry pyridine (5 mL) was added acetic anhydride (0.42 mL, 4.5 mmol). After 4.5 hours at ambient temperature, the mixture was partitioned between 1N aqueous NaHSO4 (25 mL) and EtOAc (25 mL). The EtOAc layer was washed with 1N pH7 phosphate buffer (25 mL) two times, H2O (25 mL), and brine (25 mL), dried over Na2SO4, and evaporated to give 0.91 g (100%) of 2-acetoxy-1-(4(S)-benzyl-2,2-dimethyl-oxazolidin-3-yl)-2-[1-(biphenyl-4-yl)-1H-pyrrol-3-yl]-ethanone as an amorphous solid that was used without further purification. An analytical sample was obtained upon flash column chromatography with 0-2% EtOAc/CH2Cl2 gradient eluent.

1. customthe mixture was partitioned between 1N aqueous NaHSO4 (25 mL) and EtOAc (25 mL)
2. washThe EtOAc layer was washed with 1N pH7 phosphate buffer (25 mL) two times, H2O (25 mL), and brine (25 mL)
3. dry with materialdried over Na2SO4
4. customevaporated