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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(2,4-dichlorophenyl)but-3-en-2-one | HCID 3518964 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 2,2-Diethylpropanedioate | HCID 6951563 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-(2,4-Dichlorophenyl)cyclohexane-1,3-dione | HCID 599128 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04291034 |
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| Source dataset | uspto-grants-1981_09 |
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| ORD ID | ord-60527b318a9f4f77a88210cd8de47ffc |
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| Source note | uspto-grants-1981_09 |
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