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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989796Generated: November 1, 2026

1,2-Dichloroethane → Ethyl 2,4,5-trifluorobenzoylacetate

https://huagongshe.com/reaction/1989796

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantHydrochloric AcidHCID 313—
Reactant2,4,5-TrifluorobenzonitrileHCID 593813—
ReactantPotassium ethylmalonateHCID 86617294—
CatalystZincchlorideHCID 3007855—
ProductEthyl 2,4,5-trifluorobenzoylacetateHCID 275893380%

Reaction Conditions

Temperature90 °C

Reaction Steps

To 10 □ of 1,2-dichloroethane were added 1.0 g of 2,4,5-trifluorobenzonitrile, 0.43 g of zinc chloride, and 1.3 g of potassium ethylmalonate, and then the mixture was stirred at reflux. After the reaction was completed, 11 □ of 6 N hydrochloric acid 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=1/10, v/v) to obtain the title compound in the yield of 80% (1.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642356B2
Source datasetuspto-grants-2010_01
ORD IDord-0a34a13c737c42d29ed0201a6542d316
Source noteuspto-grants-2010_01