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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296957Generated: October 30, 2026

Benzyl Bromide → HCID 58913484, compound

https://huagongshe.com/reaction/1296957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 11277788HCID 11277788—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 58913484HCID 58913484—

Reaction Steps

1-(5-Chloro-2,4-dihydroxy-phenyl)-2-(4-methoxy-phenyl)-ethanone (1 eq) was dissolved in acetonitrile and potassium carbonate (4 eq) was added portion wise. The suspension was stirred for five minutes, before the addition of benzyl bromide (2.4 eq), and after which, the reaction mixture was stirred under nitrogen at reflux for 3 hours. The reaction was allowed to cool to room temperature and diluted with water. This was extracted into ethyl acetate. The organic phase was dried over MgSO4, filtered and concentrated in vacuo to give a syrup. This was triturated with 1:1 diethyl ether:hexane to give 1-(2,4-bis-benzyloxy-5-chloro-phenyl)-2-(4-methoxy-phenyl)-ethanone as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07247734B2
Source datasetuspto-grants-2007_07
ORD IDord-1c21046a8a7a4ef9bb5c93385ee8fa15
Source noteuspto-grants-2007_07