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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72298Generated: October 29, 2026

Hydrochloric Acid → 3-(4'-Chloro-3-methylbiphen-4-yl)bicyclo[3.2.1]octane-2,4-dione

https://huagongshe.com/reaction/72298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTolueneHCID 1140—
ReactantChloroformHCID 6212—
ReactantHCID 178476523HCID 178476523—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Product3-(4'-Chloro-3-methylbiphen-4-yl)bicyclo[3.2.1]octane-2,4-dioneHCID 131731832—

Reaction Conditions

Temperature80 °C

Reaction Steps

Bicyclo[3.2.1]-2,4-dione (0.20 g, 1.44 mmol) and 4-dimethylaminopyridine (0.88 g, 7.21_mmol) are added to a mixture of chloroform (4 ml) and toluene (1 ml), and the reaction mixture is flushed with nitrogen for 15 minutes at ambient temperature. 4′-Chloro-3-methylbiphen-4-yllead triacetate (0.95 g, 1.6 mmol) is added in one portion and the reaction mixture is stirred and heated to 80° C. under an atmosphere of nitrogen for 1 hour. The reaction mixture is cooled to room temperature, acidified to pH 1 with 2N aqueous hydrochloric acid, filtered through a plug of diatomaceous earth and the two phases separated. The aqueous phase is extracted with dichloromethane (2×5 ml), the organic phases are combined, washed with water, and dried over anhydrous sodium sulfate. The mixture is filtered, and the filtrate is evaporated under reduced pressure. The residue is purified by column chromatography on silica gel to give 3-(4′-chloro-3-methylbiphen-4-yl)bicyclo[3.2.1]octane-2,4-dione.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08828908B2
Source datasetuspto-grants-2014_09
ORD IDord-3b266302d40c46c7a3e0215aa4fdbee6
Source noteuspto-grants-2014_09