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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716855Generated: November 2, 2026

Urea → Ethyl 2-amino-1,3-oxazole-4-carboxylate

https://huagongshe.com/reaction/1716855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantUreaHCID 1176—
ReactantEthyl bromopyruvateHCID 66144—
SolventEthanolHCID 702—
ProductEthyl 2-amino-1,3-oxazole-4-carboxylateHCID 31954985%

Reaction Steps

A stirred solution of ethyl bromopyruvate (50.2 g, 257.2 mmol) in EtOH was treated with urea (23.2 g, 385.8 mmol) refluxed overnight and concentrated under reduced pressure. The resultant residue was dissolved in EtOAC and water. The layers were separated and the aqueous layer washed with EtOAC. The combined organic layers were washed successively with saturated sodium chloride, dried over Mg2SO4 and concentrated under reduced pressure to give the title product in 85% yield, identified by NMR and mass spectral analyses. LCMS (ESI+) 157.1 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803825B2
Source datasetuspto-grants-2010_09
ORD IDord-da1cd99ffa3a4126abc1554071423f3f
Source noteuspto-grants-2010_09