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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170426Generated: November 2, 2026

Propargyl bromide → 1-(Prop-2-yn-1-yl)imidazolidin-2-one

https://huagongshe.com/reaction/1170426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
Reactant2-ImidazolidinoneHCID 8453—
ReactantPotassium bisulfateHCID 516920—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
Product1-(Prop-2-yn-1-yl)imidazolidin-2-oneHCID 1566965724%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a suspension of ethylene urea (592 mg, 6.88 mmol) in tetrahydrofuran (15 mL) was added dropwise butyl lithium/hexane solution (2.7 mL, 13.6 mmol) at 0° C. under nitrogen. Thereto was added 3-bromopropyne (410 mg, 6.88 mmol), and the mixture was stirred at 60° C. for 3 hours. Thereto was added 5% aqueous potassium bisulfate solution, and the mixture was extracted with ethyl acetate, dried over magnesium sulfate, and filtered. The filtrate was concentrated in vacuo and the residue was purified by silica gel chromatography (ethyl acetate/hexane 1/1) to give the titled compound (202 mg, 24%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825155B2
Source datasetuspto-grants-2010_11
ORD IDord-e8b54dab38d047f7b31bfa9daba23259
Source noteuspto-grants-2010_11