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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976604Generated: October 30, 2026

Sodium Carbonate → 5-Oxazolidinecarboxylicacid,2-oxo-,methylester(8CI,9CI)

https://huagongshe.com/reaction/1976604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantDiisopropylethylamineHCID 81531—
ReactantTriphosgeneHCID 94429—
Reactant(2R,3S)-3-amino-3-(3,4-difluorophenyl)-2-hydroxypropionic acid methyl esterHCID 57167178—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product5-Oxazolidinecarboxylicacid,2-oxo-,methylester(8CI,9CI)HCID 4292406—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (2R,3S)-3-amino-3-(3,4-difluorophenyl)-2-hydroxypropionic acid methyl ester (5.8 g, 25 mmol) in 250 mL tetrahydrofuran at 0° C. was added N,N-diisopropylethylamine (8.75 mL, 50 mmol) and triphosgene (2.48 g, 8.4 mmol). The reaction was stirred at 0° C. for 30 min when it was poured over ethyl acetate (200 mL) and saturated sodium carbonate solution (100 mL). The layers were separated, the organic layer washed with saturated sodium carbonate solution (1×100 mL), dried with magnesium sulfate, and concentrated in vacuo to provide a pale yellow oil. The material svas triturated with 25% ethyl acetate/hexane to provide (4S,5R)-4-(3,4-difluorophen)fl)-2-oxo-oxazolidine-5-carboxylic acid methyl ester. The recovered mother liquor was passed through silica (50% ethyl acetate/hexane) to give additional product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06228870B1
Source datasetuspto-grants-2001_05
ORD IDord-2a0a5bda632f4a9880c06f6fac1acb9a
Source noteuspto-grants-2001_05