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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700712Generated: November 1, 2026

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

https://huagongshe.com/reaction/1700712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
ReactantSodium ethoxideHCID 2723922—
Reactant4-(5-Chloro-2-methoxyphenyl)-3-buten-2-oneHCID 53660968—
SolventEthanolHCID 702—
Product5-(5-Chloro-2-methoxyphenyl)cyclohexane-1,3-dioneHCID 18317701—

Reaction Steps

To a solution of 20% sodium ethoxide in ethanol (2.3 g) was added at room temperature diethyl malonate (5.4 g) and then was added little by little 4-(5-chloro-2-methoxyphenyl)-3-buten-2-one (6.8 g), and the reaction mixture was stirred at room temperature for 30 minutes, refluxed for 2 hours and cooled. The solvent was evaporated, and to the residue was added water. The aqueous layer was washed with ethyl acetate and concentrated. To the residue was added 2M sodium hydroxide (18 ml), and the mixture was refluxed for 2 hours and cooled. To the mixture was added 2.5M sulfuric acid (18 ml) for 15 minutes, and the mixture was refluxed for 15 minutes, cooled and extracted with ethyl acetate. 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-(5-chloro-2-methoxyphenyl)cyclohexane-1,3-dione (7.3 g) as amorphous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350749B1
Source datasetuspto-grants-2002_02
ORD IDord-3e99606bc58c448ab61e54d7e0e90cd2
Source noteuspto-grants-2002_02