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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537674Generated: October 26, 2026

Toluene → 3-(5-Bromo-2-ethylphenyl)bicyclo[3.2.1]octane-2,4-dione

https://huagongshe.com/reaction/537674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantBicyclo(3.2.1)octane-2,4-dioneHCID 144686—
ReactantHCID 178476533HCID 178476533—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventChloroformHCID 6212—
Product3-(5-Bromo-2-ethylphenyl)bicyclo[3.2.1]octane-2,4-dioneHCID 66679569—

Reaction Steps

To a solution of 5-bromo-2-ethylphenyllead triacetate (16.34 g, 28.80 mmol) in chloroform (160 ml) is added bicyclo[3.2.1]octane-2,4-dione (3.61 g, 26.10 mmol) and 4-dimethylaminopyridine (16.63 g, 131 mmol), and the reaction mixture is stirred at room temperature for 5 minutes. Next toluene (40 ml) is added, and the mixture is stirred at 80° C. for 1 hour (pre-heated oil bath). The reaction mixture is allowed to cool to room temperature, quenched with 1M hydrochloric acid, and the organic phase separated. The aqueous phase is further washed with dichloromethane (×2), and again the phases are separated. All organics are combined then evaporated under reduced pressure to give a crude oil, which is purified by flash column chromatography on silica gel (30% to 50% ethyl acetate/iso-hexane eluant ratio, then 10% methanol/dichloromethane eluant ratio). The resulting gum is then recrystalised from dichloromethane/hexane to afford 3-(5-bromo-2-ethylphenyl)bicyclo[3.2.1]octane-2,4-dione as a cream coloured solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865623B2
Source datasetuspto-grants-2014_10
ORD IDord-9eccd53d83b44bd58acb53372cce2fd2
Source noteuspto-grants-2014_10