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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846647Generated: October 31, 2026

Propargyl bromide → 1-Methyl-3-(2-propynyl)-2-imidazolidinone

https://huagongshe.com/reaction/846647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantPotassium hydrideHCID 82127—
Reactant1-Methylimidazolidin-2-oneHCID 567600—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product1-Methyl-3-(2-propynyl)-2-imidazolidinoneHCID 11355513—

Reaction Steps

A suspension of potassium hydride (10.44 g of a 35% by wt suspension in mineral oil, washed with ether to remove oil, 0.09 mol) in dry THF (50 mL) was added dropwise, with cooling, to a stirred solution of 1-methyl-2-imidazolidinone (7.6 g, 0.076 mol) in dry THF (150 mL). After warming to room temperature and stirring for 20 min, the reaction was cooled again and propargyl bromide (13.54 g of an 80% solution in toluene, 0.09 mol) was added dropwise. The reaction was then allowed to slowly warm to room temperature and was stirred for 0.5 hr. The reaction was quenched with methanol and water and the solvents were removed under reduced pressure. The residual oil was partitioned between ethyl acetate and water; evaporation of the organic phase gave 10.65 g crude product. The compound was purified by chromatography on silica gel in chloroform to get 4.51 g of crystalline product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05137905
Source datasetuspto-grants-1992_08
ORD IDord-6f1c003a593f4327a321a486eb18a7c5
Source noteuspto-grants-1992_08