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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9255Generated: October 25, 2026

Acetone → 2,6-Diallyl4-benzyloxyphenol

https://huagongshe.com/reaction/9255

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 numberUS07091230B2
Source datasetuspto-grants-2006_08
ORD IDord-1782f4c6e18d44388356e24fbc39135b
Source noteuspto-grants-2006_08