HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700715Generated: October 31, 2026
Diethyl Malonate → 5-(5-Fluoro-2-methylphenyl)cyclohexane-1,3-dione
https://huagongshe.com/reaction/1700715
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 4-(5-Fluoro-2-methylphenyl)-3-buten-2-one | HCID 54039642 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-(5-Fluoro-2-methylphenyl)cyclohexane-1,3-dione | HCID 18317771 | — |
Reaction Steps
To a solution of 20% sodium ethoxide in ethanol (5.9 g) was added at room temperature diethyl malonate (14.0 g), and then added little by little 4-(5-fluoro-2-methylphenyl)-3-buten-2-one (13.4 g), and the mixture was stirred at room temperature for 30 minutes and then for 2 hours while heating, 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 (46 ml), and the mixture was refluxed for 2 hours and cooled. To the mixture was added 2.5M sulfuric acid (46 ml) for 10 minutes, and the mixture was refluxed for 30 minutes and cooled. Precipitated crystals were filtered and washed with water and isopropylether to give 5-(5-fluoro-2-methylphenyl)cyclohexane-1,3-dione (8.6 g) as colorless crystals.
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-0c7dbcbac66b43a3b27bae156f188401 |
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| Source note | uspto-grants-2002_02 |
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