Hydrogen Peroxide → HCID 11183134, compound

To a 0° C. solution of (4S)-3-[(2S)-2,3-dimethyl-3-phenylbutanoyl]-4-isopropyl-1,3-oxazolidin-2-one (0.13 g, 0.43 mmol, from Reference Example 24) in tetrahydrofuran (6 mL) and water (2 mL) is added 30% aqueous hydrogen peroxide (2.4 mL). After one to two minutes of stirring, lithium hydroxide monohydrate (36 mg) is added and the reaction mixture is allowed to stir overnight while warming to room temperature. On the following day, the reaction mixture is cooled to 0° C. and aqueous sodium sulfite solution (1.5 M, 1.3 mL) is added. After stirring for an hour at room temperature, the reaction mixture is concentrated under reduced pressure. The aqueous residue is extracted twice with dichloromethane, then acidified to pH 1 with 10% aqueous hydrochloric acid solution. The acidified aqueous phase is then extracted thrice with ethyl acetate. The combined organic extracts are washed with saturated aqueous sodium chloride, dried over anhydrous sodium sulfate, decanted, and concentrated under reduced pressure to give a white crystalline solid (60 mg, 72%). Mp 69-72° C. MS (ES−): (M−H)=191.0

1. stirringto stir overnight
2. temperatureOn the following day, the reaction mixture is cooled to 0° C.
3. stirringAfter stirring for an hour at room temperature
4. concentrationthe reaction mixture is concentrated under reduced pressure
5. extractionThe aqueous residue is extracted twice with dichloromethane
6. extractionThe acidified aqueous phase is then extracted thrice with ethyl acetate
7. washThe combined organic extracts are washed with saturated aqueous sodium chloride
8. dry with materialdried over anhydrous sodium sulfate
9. customdecanted
10. concentrationconcentrated under reduced pressure

ORD record

ord-8ae235cdee7449e3a61d9dd3f20b54fb

Source dataset

uspto-grants-2008_06

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07390910B2