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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856127Generated: October 30, 2026

Water → 1-(4-Chlorobenzyl)-3-(2-methyl-2-oxiranylmethyl)imidazolidin-2-one

https://huagongshe.com/reaction/856127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant2-Imidazolidinone, 1-((4-chlorophenyl)methyl)-HCID 5076481—
Reactant2-Methyloxiran-2-ylmethyl paratoluenesulfonateHCID 14237194—
SolventDimethylformamideHCID 6228—
Product1-(4-Chlorobenzyl)-3-(2-methyl-2-oxiranylmethyl)imidazolidin-2-oneHCID 8660479960%

Reaction Steps

Sodium hydride (99 mg, 2.49 mmol) was added to a solution of 2-methyl-2-oxiranylmethyl toluene-4-sulfonate (500 mg, 2.37 mmol) in DMF (5 ml) while cooling in an ice-bath, and the mixture was stirred at room temperature for 1 hour. To which a solution of 1-(4-chlorobenzyl)imidazolidin-2-one (633 mg, 2.61 mmol) in DMF (5 ml) was added while cooling in an ice-bath, and the mixture was stirred at room temperature overnight. Water was added to the reaction mixture, and the mixture was extracted with diethyl ether twice. The extracts were combined, washed with water twice and then with brine, and dried over sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/acetone=3/1) to afford 1-(4-chlorobenzyl)-3-(2-methyl-2-oxiranylmethyl)imidazolidin-2-one (399 mg, 60%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-ddd6fd6ea5c74b74a1315829a27ac8dc
Source noteuspto-grants-2007_08