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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474008Generated: October 26, 2026

Ethyl bromopyruvate → Ethyl 2-(3-hydroxy-4-methylphenylamino)oxazole-4-carboxylate

https://huagongshe.com/reaction/1474008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
Reactant(3-Hydroxy-p-tolyl)ureaHCID 85554—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-(3-hydroxy-4-methylphenylamino)oxazole-4-carboxylateHCID 6849144350%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution containing 1-(3-hydroxy-4-methylphenyl)urea (150 mg, 0.9 mmol) and ethyl 3-bromopyruvate (0.11 mL, 0.9 mmol) in dry DMF (3.611E) was heated at 60° C. for 6 h. The reaction mixture was diluted with EtOAc and washed with brine and saturated NaHCO3 solution and the combined organic layers were dried (Na2SO4) and concentrated. The crude product was purified by flash chromatography on silica gel (hexane:EtOAc 6/4) to give the product in 50% yield (119 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018209B2
Source datasetuspto-grants-2015_04
ORD IDord-5190e91344024ebea7a6c9abb9757fb5
Source noteuspto-grants-2015_04