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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727291Generated: October 26, 2026

Acetone → 2,6-Diallyl4-benzyloxyphenol

https://huagongshe.com/reaction/1727291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantMonobenzoneHCID 7638—
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Product2,6-Diallyl4-benzyloxyphenolHCID 21985951—

Reaction Steps

To a solution of starting 4-benzyloxyphenol (20 g) in acetone (800 mL) were added allylbromide (50 mL) and K2CO3 (60 g). The reaction mixture was refluxed overnight. After cooling to the room temperature, the insoluble materials were removed by filtration. The filtrate was concentrated in vac. The residue was partitioned between ethyl ether (500 mL) and 2N aqueous NaOH (200 mL). The organic layer was washed with water and brine, dried over anhydrous MgSO4, filtered, and concentrated in vac. to give the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495020B2
Source datasetuspto-grants-2009_02
ORD IDord-7db7d11367db4196b7ba4f3b41e230f5
Source noteuspto-grants-2009_02