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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358382Generated: October 27, 2026

2-Hydroxy-4-methoxybenzophenone → {4-Methoxy-2-[(prop-2-en-1-yl)oxy]phenyl}(phenyl)methanone

https://huagongshe.com/reaction/358382

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Hydroxy-4-methoxybenzophenoneHCID 4632—
ReactantPotassium IodideHCID 4875—
ReactantAllyl chlorideHCID 7850—
ReactantPotassium HydroxideHCID 14797—
SolventTetrahydrofuranHCID 8028—
Product{4-Methoxy-2-[(prop-2-en-1-yl)oxy]phenyl}(phenyl)methanoneHCID 14227056—

Reaction Steps

2-Hydroxy-4-methoxybenzophenone (114 parts) was dissolved in tetrahydrofuran (100 parts). Potassium hydroxide (30.9 parts) was added. By heating and stirring, complete dissolution was achieved. Allyl chloride (46.4 parts) and potassium iodide (4.2 parts) were added to this solution, which was then heated and refluxed for 8 hours. After cooling, it was washed with water and the solvent was removed by distillation. A crude product of the desired 2-allyloxy-4-methoxybenzophenone was obtained. It was recrystallized in n-hexane to obtain 125 parts of 2-allyloxy-4-methoxybenzophenone (melting point 40° C.) at 93% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04467082
Source datasetuspto-grants-1984_08
ORD IDord-b194dbbb179640d88942b8ef085f31a9
Source noteuspto-grants-1984_08