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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710128Generated: November 2, 2026

Propargyl bromide → HCID 15086767, compound

https://huagongshe.com/reaction/1710128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantSodium hydrideHCID 24758—
Reactant(S)-3-((tert-Butyldimethylsilyl)oxy)pyrrolidin-2-oneHCID 10584804—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15086767HCID 15086767—

Reaction Conditions

Temperature0 °C

Reaction Steps

In one portion, 11.6 g of (S)-3-[[(1,1-dimethyl-ethyl)dimethylsilyl]oxy]-2-pyrrolidinone was added to a suspension of 2.35 g of 60% sodium hydride in mineral oil in 400 ml of tetrahydrofuran which was cooled to 0° C. The resulting solution was stirred at room temperature until solution was complete, then recooled to 0° C. An 80% solution of propargyl bromide in toluene (8.5 ml) was added and the resulting solution was stirred overnight. The solution was diluted with dichloromethane, washed with water, dried and concentrated in vacuo. The residue was purified by chromatography (silica gel), giving (S)-3-[[(1,1-dimethylethyl)-dimethylsilyl]oxy]-1-(2-propynyl)-2-pyrrolidinone, [α]D26 =-44° (dichloromethane); mp 35°-36° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04952600
Source datasetuspto-grants-1990_08
ORD IDord-945eb2522ae240429fc3f0c13d8a4a6a
Source noteuspto-grants-1990_08