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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 4-(5-Chloro-2-methoxyphenyl)-3-buten-2-one | HCID 53660968 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-(5-Chloro-2-methoxyphenyl)cyclohexane-1,3-dione | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06350749B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-3e99606bc58c448ab61e54d7e0e90cd2 |
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| Source note | uspto-grants-2002_02 |
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