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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010610Generated: October 30, 2026

Ethyl bromopyruvate → HCID 59384155, compound

https://huagongshe.com/reaction/1010610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86630118HCID 86630118—
ReactantHCID 178466608HCID 178466608—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 59384155HCID 59384155—

Reaction Steps

Ethel 1-(3-ethoxyphenyl)-2-(2-fluoro-4-methylphenyl)-1H-imidazole-4-carboxylate. To a mixture of the compound from Step A and 0.80 g (9.5 mmol) of sodium bicarbonate in 10 mL of 1,4-dioxane was added 0.60 mL (4.8 mmol) of ethyl bromopyruvate. The reaction mixture was refluxed overnight. After cooling to room temperature, the solid was filtered off and the filtrate was concentrated in vacuo. Flash chromatography on a Biotage Horizon® system (silica gel, 0 to 50% ethyl acetate in hexanes gradient) gave the title compound as a viscous yellow oil. LC/MS 369.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977339B2
Source datasetuspto-grants-2011_07
ORD IDord-9f106efea9b64bafb914789a28a707ed
Source noteuspto-grants-2011_07