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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401272Generated: November 1, 2026

Ethyl bromoacetate → Ethyl[(55)-3-(2,4-dimethoxybenzyl)-2-oxo-5-(propan-2-yl)imidazolidin-1-yl]acetate

https://huagongshe.com/reaction/2401272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
Reactant(S)-1-(2,4-dimethoxybenzyl)-4-isopropylimidazolidin-2-oneHCID 67033222—
SolventDimethylformamideHCID 6228—
ProductEthyl[(55)-3-(2,4-dimethoxybenzyl)-2-oxo-5-(propan-2-yl)imidazolidin-1-yl]acetateHCID 90321857—

Reaction Steps

Sodium hydride (60%, 380 mg) was added to a solution of (4S)-1-(2,4-dimethoxybenzyl)-4-(propan-2-yl)imidazolidin-2-one (2.4 g) in DMF (35 mL), and the mixture was stirred for 20 min. Ethyl bromoacetate (1.14 mL) was added thereto, and the mixture was stirred at 90° C. for 1 hr. Additional ethyl bromoacetate (1.14 g) and sodium hydride (60%, 380 mg) were added thereto, and the resulting mixture was further stirred at 90° C. for 1 hr. After the solvent was distilled off under reduced pressure, the residue was purified by column chromatography (silica gel cartridge, hexane/ethyl acetate) to afford ethyl[(55)-3-(2,4-dimethoxybenzyl)-2-oxo-5-(propan-2-yl)imidazolidin-1-yl]acetate (1.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796272B2
Source datasetuspto-grants-2014_08
ORD IDord-5888cc7f2a17463d9bf7d9e15924fcec
Source noteuspto-grants-2014_08