Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003935Generated: October 31, 2026

Allyl bromide → HCID 10601391, compound

https://huagongshe.com/reaction/1003935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant209746-56-5HCID 6918439—
SolventAcetoneHCID 180—
ProductHCID 10601391HCID 1060139160%

Reaction Steps

3-(5-Benzo[b]furanyl)-2'-(β-D-glucopyranosyloxy)-6'-hydroxy-4'-methylpropiophenone (2.50 g) is dissolved in acetone (20 ml), and thereto are added potassium carbonate (2.13 g) and allyl bromide (933 mg), and the mixture is refluxed for 6 hours. After cooling, the reaction mixture is poured into ice-water, and the mixture is extracted with ethyl acetate. The organic layer is washed with water, dried, and concentrated under reduced pressure. The resulting residue is purified by silica gel column chromatography (solvent; chloroform/methanol) to give 3-(5-benzo[b]furanyl)-2'-(β-D-glucopyranosyloxy)-6'-allyloxy-4'-methylpropiophenone (1.63 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06048842
Source datasetuspto-grants-2000_04
ORD IDord-22413ed291b94becb6f3eb1d406f315a
Source noteuspto-grants-2000_04