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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305645Generated: November 1, 2026

Trifluoroacetic acid → 5-(S)-azidomethyl-3-(4'-carboxy-3'-fluorophenyl)oxazolidine-2-one

https://huagongshe.com/reaction/2305645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant5-(S)-azidomethyl-3-[4'-tert-butoxycarbonyl-3'-fluorophenyl]oxazolidine-2-oneHCID 22966217—
SolventDichloromethaneHCID 6344—
Product5-(S)-azidomethyl-3-(4'-carboxy-3'-fluorophenyl)oxazolidine-2-oneHCID 22966209—

Reaction Steps

60% TFA in DCM (5 mL) was added to 5-(S)-azidomethyl-3-[4′-tert-butoxycarbonyl-3′-fluorophenyl]oxazolidine-2-one (0.336 g, 1 mmol), and the solution kept at r.t. for 1 h. Solvents were removed in vacuo to afford 5-(S)-azidomethyl-3-[4′-carboxy-3′-fluorophenyl-)oxazolidine-2-one dried (0.280 g, 99%). N-Trimethylsilyl-N,N-diethylamine (0.23 mL, 1.2 mmol) was added to above product in dry dichloromethane (3 mL) under nitrogen atmosphere, and the solution stirred for 15 min. Solvents and excess reagent were removed in vacuo, and residue dissolved in dichloromethane (4 mL). The solution was cooled to about 0° C., and oxalyl chloride (1.5 mmol, 0.13 mL) was added dropwise, followed by catalytic N,N-dimethylformamide (about 0.01 mL). The mixture was alllowed to warm up to r.t. (room temperature), and stirred at r.t. for another 2 h. Solvents were removed in vacuo to afford the product as a white solid. Yield 0.292 g (98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441005B1
Source datasetuspto-grants-2002_08
ORD IDord-aba1d890779741bfa59b4f96d3e69207
Source noteuspto-grants-2002_08