HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57379Generated: October 25, 2026
Ammonia → (S)-4-((R)-1,1-difluoropropan-2-yl)oxazolidin-2-one
https://huagongshe.com/reaction/57379
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | (S)-3-benzyl-4-((R)-1,1-difluoropropan-2-yl)oxazolidin-2-one | HCID 90414714 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (S)-4-((R)-1,1-difluoropropan-2-yl)oxazolidin-2-one | HCID 90416634 | 88.1% |
Reaction Steps
To liquid ammonia at −50° C. under argon was slowly added a solution of (S)-3-benzyl-4-((R)-1,1-difluoropropan-2-yl)oxazolidin-2-one (627 mg) (200 mg, 0.784 mmol) in diethylether (10 mL). Lithium (pellets; 54.4 mg, 7.84 mmol) were added in three portions. The reaction mixture became green then dark greenish blue over ˜10 min. The mixture was stirred for additional 15 min and then quenched slowly by the addition of saturated aqueous ammonium chloride solution (3 mL). The mixture was allowed to warm slowly to room temperature. The residue was diluted with diethylether (20 mL) and water (10 mL). The separated aqueous layer was extract with ether (2×25 mL) and DCM (3×20 mL). The DCM and ether layers were separately concentrated under reduced pressure. The residues were dissolved in DCM and combined. The organic layer was dried over magnesium sulfate, filtered off and concentrated under reduced pressure providing crude (S)-4-((R)-1,1-difluoropropan-2-yl)oxazolidin-2-one (114 mg) as a colorless solid, which was directly used without further purification. MS m/z 166.1 (M+H)+; Rt-0.37 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434719B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-d647900c07fc4ddaafa5eae26d9861a6 |
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| Source note | uspto-grants-2016_09 |
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