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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49264Generated: October 29, 2026

Sodium hydride → 1-[6-(4-Bromophenoxy)hexyl]-3-(4-fluorophenyl)-2-imidazolidinone

https://huagongshe.com/reaction/49264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-(4-Fluorophenyl)imidazolidin-2-oneHCID 1480785—
ReactantHCID 20636597HCID 20636597—
SolventDimethylformamideHCID 6228—
Product1-[6-(4-Bromophenoxy)hexyl]-3-(4-fluorophenyl)-2-imidazolidinoneHCID 12986487—

Reaction Steps

To a solution of 1-(4-fluorophenyl)-2-imidazolidinone (0.12 g, 0.65 mmol) dissolved in 10 mL dimethylformamide cooled in an ice bath was added NaH (60% dispersion in mineral oil, 39.0 mg, 0.98 mmol). The mixture was stirred at room temperature for 30 minutes and then cooled in ice bath. 1-Bromo-6-(4-bromophenoxy)heptane (0.22 g, 0.65 mmol) was added, and the mixture was stirred at room temperature for additional 4 hours. The reaction was quenched with methanol, and the solvents were removed under reduced pressure. 5 mL of saturated NH4Cl water solution and 10 mL of dichloromethane were added to the residue. The dichloromethane layer was dried over MgSO4, filtered, evaporated, and purified by column chromatography (ethyl acetate:MeOH=10:1) to give the product (i.e., Compound 7) as a white solid (0.14 g, 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706739B2
Source datasetuspto-grants-2004_03
ORD IDord-7070ec48c1e54d5e9696f57c6b0256e5
Source noteuspto-grants-2004_03