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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1745865Generated: October 30, 2026

Allyl bromide → HCID 22227278, compound

https://huagongshe.com/reaction/1745865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactantp-(Benzyloxy)phenethyl alcoholHCID 3017260—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 22227278HCID 22227278—

Reaction Conditions

Temperature50 °C

Reaction Steps

A reaction flask was charged with 4-benzyloxy phenethyl alcohol of formula (6), (12 g, 0.052 mol), potassium tert-butoxide (8.842 g, 0.079 ml) and 50 ml and DMSO. The mixture was stirred under nitrogen at 50° C. for 30 minutes. A solution of allyl bromide (6.8 ml, 0.079 mol) was added drop wise to the reaction mixture with cooling about 20–25° C. The mixture was then stirred at 50° C. for 2 h. and cooled to room temperature. The reaction mixture was subsequently quenched with 150 ml of water. The desired product was extracted from neutralized aqueous mixture with toluene. The toluene extract was then washed with water and concentrated under vacuum to afford the title compound of formula (7), 13.9 g, (98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07019172B2
Source datasetuspto-grants-2006_03
ORD IDord-e848b7d491d046428efb2c46b23ffb9a
Source noteuspto-grants-2006_03