HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539098Generated: October 30, 2026
Potassium Hydroxide → (S)-4-(5-fluoropyridin-2-yl)oxazolidin-2-one
https://huagongshe.com/reaction/539098
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | (S)-2-Amino-2-(5-fluoropyridin-2-yl)ethan-1-ol dihydrochloride | HCID 67033052 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (S)-4-(5-fluoropyridin-2-yl)oxazolidin-2-one | HCID 67033294 | 55.8% |
Reaction Steps
To the solution of (S)-2-amino-2-(5-fluoropyridin-2-yl)ethanol bis-hydrochloride (9.8 g, 43 mmol) in water (200 mL) cooled to 0° C. was added potassium hydroxide (24 g, 430 mmol) followed by THF (200 mL) and the reaction stirred until the temperature reached 0° C. To the reaction was added bis(trichloromethyl) carbonate (13 g, 43 mmol) (in THF, 200 mL) dropwise such that the internal temperature did not exceed 7° C., and the reaction was stirred for 2 hours. The reaction was diluted with ethyl acetate and the aqueous layer made basic with NaOH (1M). The organic layer was washed with brine, dried over MgSO4 and concentrated in vacuo. The crude material was chromatographed using a gradient of 50% DCM/EtOAc to EtOAc as eluent to yield (S)-4-(5-fluoropyridin-2-yl)oxazolidin-2-one (4.3 g, 24 mmol, 55% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865726B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-99a7f2385dca40699c4a1f952f12eb87 |
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| Source note | uspto-grants-2014_10 |
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