HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700468Generated: November 3, 2026
Chloroacetone → 6-(2,3-Dichlorophenyl)-3-methyl-4,5,6,7-tetrahydrobenzofuran-4-one
https://huagongshe.com/reaction/1700468
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 5-(2,3-Dichlorophenyl)cyclohexane-1,3-dione | HCID 18317318 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-(2,3-Dichlorophenyl)-3-methyl-4,5,6,7-tetrahydrobenzofuran-4-one | HCID 18317730 | — |
Reaction Steps
To a solution of 5-(2,3-dichlorophenyl)cyclohexane-1,3-dione(mp205-206° C.; 1.29 g) in ethanol (10 ml) was added sodium ethoxide (0.37 g), and the mixture was stirred, under argon atmosphere, at room temperature for 15 minutes. To the mixture was added a solution of chloroacetone (0.45 ml) in DMF (10 ml), and the mixture was stirred at 100° C. overnight (13 hours). The reaction solution was cooled and concentrated under reduced pressure. To the residue was added ice-water, and the mixture was extracted with ethyl acetate. The upper layer was washed with saturated brine, dried (anhydrous magnesium sulfate), and concentrated under reduced pressure, and the residue was subjected to silica gel chromatography and eluted with ethyl acetate/hexane to give 6-(2,3-dichlorophenyl)-3-methyl-4,5,6,7-tetrahydrobenzofuran-4-one (0.18 g).
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-4b99a25338da4556b4c4624f1619eecc |
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| Source note | uspto-grants-2002_02 |
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