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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704354Generated: October 27, 2026

Ethyl bromoacetate → Ethyl p-[5-(1-imidazolyl)pentyloxy]phenoxyacetate

https://huagongshe.com/reaction/704354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
Reactant4-{[5-(1H-Imidazol-1-yl)pentyl]oxy}phenolHCID 13219140—
SolventDimethylformamideHCID 6228—
ProductEthyl p-[5-(1-imidazolyl)pentyloxy]phenoxyacetateHCID 14327317—

Reaction Steps

To a solution of 2.46 g p-[5-(1-imidazolyl)pentyloxy]phenol and 1.2 ml ethyl bromoacetate in 25 ml anhydrous N,N-dimethylformamide, was added under ice cooling and with stirring 440 mg of 60% sodium hydride in oil, and stirring was continued at room temperature for ten minutes. The solvent was distilled off, the residue was dissolved in chloroform, and the solution was washed with water and dried over anhydrous sodium sulfate. After distilling off, the chloroform, the residue was purified by silical gel column chromatography, affording 2.7 g of ethyl p-[5-(1-imidazolyl)pentyloxy]phenoxyacetate as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04987147
Source datasetuspto-grants-1991_01
ORD IDord-69e8f2b20e2f42b594b8a696e47a8d02
Source noteuspto-grants-1991_01