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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722352Generated: October 30, 2026

Benzyl Chloride → HCID 14421497, compound

https://huagongshe.com/reaction/1722352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 14421495HCID 14421495—
SolventAcetoneHCID 180—
ProductHCID 14421497HCID 1442149792%

Reaction Steps

90 g (0.44 mol) of 2-allyl-6-cyclopentylphenol, 62 g (0.49 mol) of benzyl chloride and 124 g (0.9 mol) of potassium carbonate are heated under reflux in 800 ml of acetone for 70 h. The cooled reaction mixture is filtered, and the filtrate is concentrated. The residue is taken up in petroleum ether, and the solution is washed three times with 2N sodium hydroxide solution and then once each with water and saturated brine. The organic phase is dried over sodium sulfate and concentrated in vacuo. The residue is distilled in vacuo. 118 g (92% of theory) of 1-allyl-2-benzyloxy-3-cyclopentylbenzene are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04855323
Source datasetuspto-grants-1989_08
ORD IDord-fa2e6de974884a09a12d7dd67c4afba4
Source noteuspto-grants-1989_08