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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700760Generated: November 1, 2026

Diethyl Malonate → 5-(2-Chloro-5-fluorophenyl)cyclohexane-1,3-dione

https://huagongshe.com/reaction/1700760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
ReactantSodium ethoxideHCID 2723922—
Reactant4-(2-Chloro-5-fluorophenyl)-3-buten-2-oneHCID 53922918—
SolventEthanolHCID 702—
Product5-(2-Chloro-5-fluorophenyl)cyclohexane-1,3-dioneHCID 18317679—

Reaction Steps

To a solution of 20% sodium ethoxide in ethanol (0.43 g) was added at room temperature diethyl malonate (0.2 g), and then added little by little 4-(2-chloro-5-fluorophenyl)-3-buten-2-one (0.24 g). The mixture was stirred at room temperature for 30 minutes, refluxed for 2 hours and cooled, and the solvent was evaporated. The residue was dissolved in water, and the aqueous layer was washed with ethyl acetate and concentrated. To the reside was added 2M sodium hydroxide (0.7 ml), and the mixture was refluxed for 2 hours cooled. To the mixture was added 2.5M sulfuric acid (0.7 ml), and the mixture was refluxed for 15 minutes. The mixture was extracted with ethyl acetate, and the organic layer was washed with water and saturated brine and dried with magnesium sulfate. Under reduced pressure, the solvent was evaporated to give 5-(2-chloro-5-fluorophenyl)cyclohexane-1,3-dione (0.17 g) as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350749B1
Source datasetuspto-grants-2002_02
ORD IDord-3609b4ffbd5841a5b981e37b6dbe02bc
Source noteuspto-grants-2002_02