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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429879Generated: October 30, 2026

Ethyl Acetate → (4S,5R) 4-(3,4-difluorophenyl)-5-hydroxymethyl-oxazolidin-2-one

https://huagongshe.com/reaction/429879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium BicarbonateHCID 516892—
ReactantLithium borohydrideHCID 4148881—
Reactant(4S,5R)-4-(3,4-difluorophenyl)-2-oxo-oxazolidine-5-carboxylic acid methyl esterHCID 57080183—
SolventTetrahydrofuranHCID 8028—
Product(4S,5R) 4-(3,4-difluorophenyl)-5-hydroxymethyl-oxazolidin-2-oneHCID 57254260—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (4S, 5R)-4-(3,4-difluorophenyl)-2-oxo-oxazolidine-5-carboxylic acid methyl ester [(200 mg, 0.8 mmol) product of Example 6, Step D] in tetrahydrofuran (10 mL) at 0° C. was added a 2 M solution of lithium borohydride in tetrahydrofuran (0.4 mL, 0.8 mmol). After stirring for 20 min at 0° C., saturated sodium bicarbonate (20 mL) was added and the mixture stirred at ambient temperature for 20 min. Ethyl acetate (50 mL) was added and the layers separated. The organic layer was washed with brine (1×10 mL), dried with magnesium sulfate, filtered and concentrated in vacuo to provide (4S, 5R) 4-(3,4-difluorophenyl)-5-hydroxymethyl-oxazolidin-2-one as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06319932B1
Source datasetuspto-grants-2001_11
ORD IDord-685d4f1e105d424fad3c553b291fc134
Source noteuspto-grants-2001_11