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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876070Generated: October 30, 2026

Acetone → 4-Allyloxybenzophenone

https://huagongshe.com/reaction/876070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant4-HydroxybenzophenoneHCID 14347—
SolventWaterHCID 962—
Product4-AllyloxybenzophenoneHCID 25791091.9%

Reaction Steps

To start with, a three-necked flask was charged with commercially available 4-hydroxybenzophenone (39.6 g) and potassium carbonate (28 g), followed by argon substitution. Subsequently, dehydrated acetone (120 ml) was added, followed by well stirring, and then allyl bromide (18.6 ml) was added. Stirring was performed at 60° C. for 8 hours. After that, the mixture was cooled to a room temperature, and pure water was added, followed by stirring. Extraction with diethylether (100 ml) was performed twice. Extraction-and-washing with a 10% NaOH solution (100 ml) was performed twice, followed by drying over sodium sulfate. The solvent was removed by using an evaporator to obtain a pale yellow residue. The residue was recrystallized from methanol, followed by suction filtration, and then drying in vacuum was performed to obtain 4-allyloxybenzophenone (hereinafter referred to as ABP) which was a pure product (weight: 43.7 g, yield: 91.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08986488B2
Source datasetuspto-grants-2015_03
ORD IDord-6465e18953624be38c81c6114da4c063
Source noteuspto-grants-2015_03