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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Potassium hydride | HCID 82127 | — |
| Reactant | 1-Methylimidazolidin-2-one | HCID 567600 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Methyl-3-(2-propynyl)-2-imidazolidinone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05137905 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-6f1c003a593f4327a321a486eb18a7c5 |
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| Source note | uspto-grants-1992_08 |
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