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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537670Generated: October 30, 2026

Hydrochloric Acid → HCID 49765293, compound

https://huagongshe.com/reaction/537670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTolueneHCID 1140—
Reactant1,3-CyclohexanedioneHCID 10434—
ReactantHCID 178476533HCID 178476533—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventChloroformHCID 6212—
ProductHCID 49765293HCID 49765293—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 5-bromo-2-ethylphenyllead triacetate (20.00 g, 35.2 mmol) (described in WO08/071,405) in chloroform (100 ml) is added cyclohexane-1,3-dione (3.94 g, 35.2 mmol) and 4-dimethylaminopyridine (22.36 g, 176 mmol). After stirring the reaction at room temperature for 5 minutes toluene (50 ml) is added and the solution is heated at 80° C. for 4 hours. After cooling to room temperature the mixture is allowed to stand overnight, followed by treatment with 2M aqueous hydrochloric acid. Following filtration of the precipitate the biphasic solution is separated, and the aqueous phase is extracted again with dichloromethane (×2). Organic fractions are combined then evaporated under reduced pressure to yield a crude product which is purified by flash column chromatography (10% ethyl acetate/hexane to 70% ethyl acetate/hexane eluant) to afford 2-(5-bromo-2-ethylphenyl)cyclohexane-1,3-dione as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865623B2
Source datasetuspto-grants-2014_10
ORD IDord-7d68571fb2e24128991a89d0db4d2ca2
Source noteuspto-grants-2014_10