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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1578087Generated: October 30, 2026

4-(2,4-dichlorophenyl)but-3-en-2-one → 5-(2,4-Dichlorophenyl)cyclohexane-1,3-dione

https://huagongshe.com/reaction/1578087

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2,4-dichlorophenyl)but-3-en-2-oneHCID 3518964—
ReactantSodiumHCID 5360545—
Reactant2,2-DiethylpropanedioateHCID 6951563—
SolventEthanolHCID 702—
Product5-(2,4-Dichlorophenyl)cyclohexane-1,3-dioneHCID 599128—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2.3 g of sodium in 200 ml of ethanol is added 15.7 g of diethylmalonate followed by a suspension of 20 g of 1-(2,4-dichlorophenyl)-1-butene-3-one in 100 ml ethanol. The mixture is heated under reflux for 2 hrs and then concentrated to dryness in vacuo. The solid is partitioned between 200 ml water and 200 ml ether. The ether layer is discarded and 20 ml 50% NaOH is added to the aqueous layer which is heated under reflux for 2 hrs. The mixture is filtered and the filtrate is made strongly acidic pH <2 with concentrated sulfuric acid. The mixture is heated on a steam bath for 2 hrs. The resulting solid is collected, pulverized and suspended in 500 ml of 10N sulfuric acid and heated on a steam bath for 2 hrs and cooled to 0° C. The solid is collected, washed with water and recrystallized from a mixture of dimethylformamide and ethyl acetate. Drying in vacuo at 80° C. for 6 hrs gives 5-(2,4-dichlorophenyl)cyclohexane-1,3dione; mp 192°-196° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04291034
Source datasetuspto-grants-1981_09
ORD IDord-60527b318a9f4f77a88210cd8de47ffc
Source noteuspto-grants-1981_09