HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1626408Erstellt: 25. Oktober 2026
Potassium Carbonate → Ethyl 7-(4-carbamoyl-2-nitrophenoxy)-6-chlorochroman-4-carboxylate
https://huagongshe.com/reaction/1626408
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 4-Chloro-3-nitrobenzamide | HCID 27942 | — |
| Edukt | Ethyl-6-chloro-7-hydroxy-3,4-dihydro-2H-chromene-4-carboxylate | HCID 53393319 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Ethyl 7-(4-carbamoyl-2-nitrophenoxy)-6-chlorochroman-4-carboxylate | HCID 67287592 | — |
Reaktionsschritte
To a stirred solution of ethyl 6-chloro-7-hydroxychroman-4-carboxylate (6.40 g, 24.9 mmol) and 4-chloro-3-nitrobenzamide in N,N′-dimethylformamide (75 mL) at ambient temperature was added potassium carbonate (8.61 g, 62.3 mmol). An argon balloon with purge valve was attached, and the stirred mixture was evacuated and purged 5 times with argon. The mixture was stirred in an oil bath at 90° C. under argon. After 15 hours the reaction mixture was cooled to ambient temperature, then poured into a reparatory funnel containing water (1000 mL) and the extracted with ether (2×1000 mL). The organic layers were combined and dried over sodium sulfate, then evaporated to give 10.5 g of brown semi-solid. The crude material was purified by silica gel column chromatography, eluting with 99/1 chloroform/methanol followed by 98/2 chloroform/methanol to provide the desired product (7.74 g, 74%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08785445B2 |
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| Quelldatensatz | uspto-grants-2014_07 |
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| ORD ID | ord-c1b39eb3f70f440594d30dc1127ef034 |
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| Quellennotiz | uspto-grants-2014_07 |
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