HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 55175Erstellt: 23. Oktober 2026
Triethylamine → 4,5-Dihydro-5-(4-nitrobenzoyl)pyrrolo[1,2-a]quinoxaline
https://huagongshe.com/de/reaction/55175
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Edukt | 4,5-Dihydropyrrolo[1,2-a]quinoxaline | HCID 11805181 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 4,5-Dihydro-5-(4-nitrobenzoyl)pyrrolo[1,2-a]quinoxaline | HCID 21837135 | — |
Reaktionsschritte
To a solution of 5 mmol of 4,5-dihydropyrrolo-[1,2-a]quinoxaline in 50 ml of methylene chloride under argon is added 10 mmol of triethylamine followed by ice bath cooling. A solution of 5 mmol of 4-nitrobenzoyl chloride in 10 ml of methylene chloride is added dropwise. Following complete addition, the ice bath is removed and the reaction mixture stirred at room temperature for 2 hours. The volatiles are removed in vacuo to give a residue which is dissolved in ethyl acetate. The solution is washed with water, 1N HCl, NaHCO3, and brine. The reaction mixture is dried with Na2SO4, filtered and evaporated in vacuo to give a solid which is purified by flash chromatography to give the desired product (from ethyl acetate) as a solid, m.p. 174°-178° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05624923 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-d3e507833ee64f788a50f63ea137b556 |
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| Quellennotiz | uspto-grants-1997_04 |
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