Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426369Generated: November 3, 2026

Furfuryl Alcohol → HCID 9833973, compound

https://huagongshe.com/reaction/1426369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFurfuryl AlcoholHCID 7361—
ReactantPropargyl bromideHCID 7842—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 9833973HCID 983397332%

Reaction Steps

To a mixture of sodium hydride (7.7 g, 190 mmol, 60% in oil) and tetrahydrofuran (100 mL) was added dropwise furfuryl alcohol (15 mL, 170 mmol) at 0° C. The reaction mixture was warmed to room temperature, N,N-dimethylformamide (30 mL) was added at that temperature, and the mixture was stirred at that temperature for 30 minutes. The reaction mixture was returned to 0° C., propargyl bromide (23 g, 190 mmol) was added at that temperature, and the mixture was stirred for 1 hour at room temperature. Water was added to the reaction mixture, which was then extracted with ethyl acetate. The organic layer was washed with brine, and the solvent was distilled away under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:heptane=1:30) to give the title compound (7.6 g, 32% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933100B2
Source datasetuspto-grants-2015_01
ORD IDord-1f4e7423c2024bbd9b0489e2230499e7
Source noteuspto-grants-2015_01