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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660909Generated: October 29, 2026

Ethyl chloroacetate → Ethyl [4-(5-chloro-2-thienyl)-3-(2-fluorobenzyl)-2-oxo-2,3-dihydro-1H-imidazol-1-yl]-acetate

https://huagongshe.com/reaction/660909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroacetateHCID 7751—
ReactantPotassium CarbonateHCID 11430—
Reactant5-(5-chloro-2-thienyl)-1-(2-fluorobenzyl)-1,3-dihydro-2H-imidazol-2-oneHCID 58012295—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductEthyl [4-(5-chloro-2-thienyl)-3-(2-fluorobenzyl)-2-oxo-2,3-dihydro-1H-imidazol-1-yl]-acetateHCID 58012258—

Reaction Steps

650 mg (2.15 mmol) of 5-(5-chloro-2-thienyl)-1-(2-fluorobenzyl)-1,3-dihydro-2H-imidazol-2-one from Example 236A, 516 mg (4.21 mmol) of ethyl chloroacetate and 582 mg (4.21 mmol) of potassium carbonate are stirred in 12 ml acetonitrile for 7 hrs at 80° C. The reaction solution is diluted with ethyl acetate and washed three times with saturated sodium chloride solution. The organic phase is dried over sodium sulphate. After filtration from the drying agent, the filtrate is concentrated in vacuo. After purification by flash chromatography over silica gel (eluent: cyclohexane/ethyl acetate first 5:1, then 1:1), 610 mg (74% of theory) of the target compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084481B2
Source datasetuspto-grants-2011_12
ORD IDord-f0c2124665ae45cc9ce4b67f4bccbb7a
Source noteuspto-grants-2011_12