HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 544150Erstellt: 25. Oktober 2026
Bromine → Ethyl 3-bromo-6(4-chlorophenyl)-4-oxo-4H-pyran-2-carboxylate
https://huagongshe.com/reaction/544150
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Bromine | HCID 24408 | — |
| Edukt | Ethyl 6-(4-chlorophenyl)-2,4-dioxo-hex-5-enoate | HCID 610034 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | Ethyl 3-bromo-6(4-chlorophenyl)-4-oxo-4H-pyran-2-carboxylate | HCID 15578373 | — |
Reaktionsschritte
A solution of bromine (7.06 ml) in chloroform (70 ml) was added dropwise to a stirred solution of ethyl 6-(4-chlorophenyl)-2,4-dioxohex-5-enoate (19.2 g) in chloroform (300 ml) at 5° to 10° C. The solution was stirred for 30 minutes at room temperature then evaporated to a yellow oil. This crude tribromide was dissolved in dimethylsulphoxide (150 ml), and 1,5-diazabicyclo[4.3.0]non-5-ene (16.9 g) was added at 20° to 25° C. The mixture was stirred for 30 minutes at room temperature then diluted with ice-water (300 ml) to precipitate a sticky brown solid. A solution of this crude product in chloroform was passed down a short column of silica-gel (100 g) and then evaporated. The residual solid was washed with ethyl acetate-petroleum ether 60°-80° C., then recrystallised from ethyl acetate-petroleum ether 60°-80° C. to give the title product as yellow needles (mp 146°-149° C.).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04448787 |
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| Quelldatensatz | uspto-grants-1984_05 |
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| ORD ID | ord-e92d421adb904295b85ca55ced490424 |
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| Quellennotiz | uspto-grants-1984_05 |
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