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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030683Generated: October 25, 2026

Allyl bromide → 2',4',6'-Trihydroxy3'-(2-propenyl)acetophenone

https://huagongshe.com/reaction/1030683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant2',4',6'-TrihydroxyacetophenoneHCID 68073—
SolventTetrahydrofuranHCID 8028—
Product2',4',6'-Trihydroxy3'-(2-propenyl)acetophenoneHCID 1436807841.5%

Reaction Steps

In 15 ml of anhydrous tetrahydrofuran was dissolved 3.0 g of 2',4',6'-trihydroxyacetophenone, and 7.4 g of anhydrous potassium carbonate was added to the solution and the mixture was stirred at room temperature for 30 minutes. Then, 2.5 g of 3-bromo-1-propene was added to the mixture and reaction was carried out at room temperature for 3 hours. After the reaction, the reaction mixture was extracted with 500 ml of diethyl ether, and the solvent was removed from the extract by distillation. The obtained residue was recrystallized from benzene to obtain 1.5 g (yield=41.5%) of 2',4',6'-trihydroxy-3'-(2-propenyl)acetophenone in the form of a colorless prism.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05106871
Source datasetuspto-grants-1992_04
ORD IDord-3fabc0dff25e41778d2397b75add0719
Source noteuspto-grants-1992_04