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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantSodium HydroxideHCID 14798—
ReactantTriphosgeneHCID 94429—
Reactant(S)-2-Amino-2-(5-fluoropyridin-2-yl)ethan-1-ol dihydrochlorideHCID 67033052—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(S)-4-(5-fluoropyridin-2-yl)oxazolidin-2-oneHCID 6703329455.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865726B2
Source datasetuspto-grants-2014_10
ORD IDord-99a7f2385dca40699c4a1f952f12eb87
Source noteuspto-grants-2014_10