Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254198Generated: October 26, 2026

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

https://huagongshe.com/reaction/2254198

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 numberUS05234951
Source datasetuspto-grants-1993_08
ORD IDord-cf394d6cdd0c4b3682acc9b302a37f5e
Source noteuspto-grants-1993_08