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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987721Generated: October 29, 2026

HCID 10424733, compound → HCID 69031029, compound

https://huagongshe.com/reaction/1987721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10424733HCID 10424733—
ReactantHCID 12433731HCID 12433731—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 69031029HCID 69031029—

Reaction Steps

N-[(4S)-3-benzyloxycarbonyl-5-oxo-oxazolidin-4-yl-acetyl chloride (3.00 g, 10 mmol) in dichloromethane (20 mL) was added dropwise to a solution of tert-butyl-N-phenylglycinate (2.3 mg, II mmol) in pyridine (10 mL) at 0 C. The reaction was allowed to warm to room temperature and stirred overnight. The reaction was diluted with H2O (100 mL) and EtOAc (150 mL). The organic phase was separated and washed successively with citric acid (10%, 2×100 mL) and brine (100 mL), dried (MgSO4), filtered and concentrated in vacuo to give a yellow viscous oil. Column chromatography (SiO2, 20-50% EtOAc in petroleum ether) gave tert-butyl N-[(4S)-3-benzyloxycarbonyl-5-oxo-oxazolidin-4-yl-acetyl]-N-phenylglycinate as a white foam. MS (APCI) m/z 467 (M+−1,100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07553809B2
Source datasetuspto-grants-2009_06
ORD IDord-6cf29afd1ab94aa6a8aff1f2eee0f72b
Source noteuspto-grants-2009_06