HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700477Generated: October 30, 2026
Ethyl bromopyruvate → HCID 18317463, compound
https://huagongshe.com/reaction/1700477
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl bromopyruvate | HCID 66144 | — |
| Reactant | 5-(2-Chlorophenyl)cyclohexane-1,3-dione | HCID 875360 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18317463 | HCID 18317463 | — |
Reaction Steps
To a solution of 5-(2-chlorophenyl)cyclohexane-1,3-dione (2.23 g) in ethanol (30 ml) was added sodium ethoxide (0.75 g), and the mixture was stirred, under argon atmosphere, at room temperature for 15 minutes. To the mixture was added ethyl bromopyruvate (1.66 ml), and the mixture was stirred, under argon atmosphere, at room temperature for 2 hours. The reaction solution was concentrated under reduced pressure, and to the residue were added DMF (30 ml) and potassium carbonate (1.38 g). The mixture was stirred, under argon atmosphere, at 150° C. overnight (14 hours). The reaction solution was cooled, and to the mixture was added ice-water. 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-chlorophenyl)-3-ethoxycarbonyl-4,5,6,7-tetrahydrobenzofuran-4-one (0.14 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-e9632cdf9fdb44b6ac0e6055c877f823 |
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| Source note | uspto-grants-2002_02 |
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