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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1498906Generated: October 31, 2026

Hydrochloric Acid → Ethyl 4-(2,4-dichlorophenyl)-2,4-dioxobutanoate

https://huagongshe.com/reaction/1498906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl OxalateHCID 7268—
Reactant2',4'-DichloroacetophenoneHCID 16693—
ReactantEthanol sodium ethoxideHCID 23706232—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-(2,4-dichlorophenyl)-2,4-dioxobutanoateHCID 2299747878.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

A 20% sodium ethoxide-ethanol solution (17 g) was added to tetrahydrofuran (100 ml), and the mixture was cooled to 0° C. It took 60 minutes to dropwise add a solution of 2′,4′-dichloroacetophenone (9.45 g) and diethyl oxalate (7.30 g) in tetrahydrofuran (100 ml) to the mixture. After the completion of the dropping, the mixture was allowed to warm to a room temperature and stirred for 2 hours. To the mixture, 2-N hydrochloric acid (200 ml) and chloroform (200 ml) were added. The organic layer was collected by separation and dried over anhydrous magnesium sulfate, and the solvent was distilled off. Thus, the title compound (11.3 g, 78%) as a light-brown oily substance was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09200008B2
Source datasetuspto-grants-2015_12
ORD IDord-8d9a8dc1f44042208113ba2f3fba5115
Source noteuspto-grants-2015_12