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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766415Generated: October 26, 2026

Ethyl bromopyruvate → 1-(4-chloro-phenyl)-2-(2-chloro-phenyl)-4-hydroxy-4,5-dihydro-1H-imidazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1766415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178512017HCID 178512017—
SolventIsopropanolHCID 3776—
Product1-(4-chloro-phenyl)-2-(2-chloro-phenyl)-4-hydroxy-4,5-dihydro-1H-imidazole-4-carboxylic acid ethyl esterHCID 58760953—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2-chloro-N-(4-chloro-phenyl)-benzamidine (I-5a), 25.1 g, 95 mmol) and NaHCO3 (84 g, 189 mmol) in 2-propanol (473 ml) was treated with 3-bromo-2-oxo-propionic acid ethyl ester (14.3 ml, 22 g, 113 mmol). The reaction mixture was heated at 80° C. for 17 hours. After cooling to room temperature, the solvent was removed in vacuo. The residue was diluted with CH2Cl2 and the organic solution was washed with H2O, dried over MgSO4, and concentrated in vacuo to provide the product, 1-(4-chloro-phenyl)-2-(2-chloro-phenyl)-4-hydroxy-4,5-dihydro-1H-imidazole-4-carboxylic acid ethyl ester I-5b, as a dark red residue (36 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230024B2
Source datasetuspto-grants-2007_06
ORD IDord-038bc1b3cdb7484292946646b37f010a
Source noteuspto-grants-2007_06