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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989798Generated: November 1, 2026

1,2-Dichloroethane → Ethyl benzoylacetate

https://huagongshe.com/reaction/1989798

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantBenzonitrileHCID 7505—
ReactantPotassium ethylmalonateHCID 86617294—
CatalystCupric ChlorideHCID 24014—
ProductEthyl benzoylacetateHCID 717068%

Reaction Conditions

Temperature90 °C

Reaction Steps

To 100 □ of 1,2-dichloroethane were added 5.5 □ of benzonitrile, 3.6 g of copper chloride and 11 g of potassium ethylmalonate, and then the mixture was stirred at reflux. After the reaction was completed, 100 □ of 6 N hydrochloric was added to the mixture, which then was stirred at reflux at 90° C. for 1 hour. After confirming completion of the reaction by TLC, the solution was cooled to 20° C., and then an organic layer was separated therefrom. The organic layer was concentrated through distillation under reduced pressure. Thus resulted residue was purified by silica gel column chromatography (eluent: ethylacetate/n-hexane=1/20, v/v) to obtain the title compound in the yield of 68% (7.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642356B2
Source datasetuspto-grants-2010_01
ORD IDord-91b9e7e280524cada39b751ba1498914
Source noteuspto-grants-2010_01