HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2184449Erstellt: 25. Oktober 2026
Pyrrole-2-carboxaldehyde → 1-[(4,5-Dimethoxy-2-nitrophenyl)methyl]-1H-pyrrole-2-carboxaldehyde
https://huagongshe.com/reaction/2184449
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Pyrrole-2-carboxaldehyde | HCID 13854 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 1-(Bromomethyl)-2-nitro-4,5-dimethoxybenzene | HCID 3016812 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 1-[(4,5-Dimethoxy-2-nitrophenyl)methyl]-1H-pyrrole-2-carboxaldehyde | HCID 310827 | 94,6% |
Reaktionsschritte
To a suspension of sodium hydride (0.724 g, 60% suspension in oil) in N,N-dimethylformamide (50 mL) was added pyrrole 2-carboxaldehyde (1.7 g, 18.1 mmol) and the reaction mixture was stirred for 30 minutes. It was then cooled to 0° C. and 4,5-dimethoxy-2-nitrobenzyl bromide (5.0 g, 1 equiv) was added dropwise over 20 minutes. After the addition, the reaction mixture was stirred at room temperature for 3 hours. It was then diluted with ethyl acetate (450 mL), washed with water, dried over anhydrous magnesium sulfate, filtered and evaporated to dryness. The crude product was triturated with water, filtered and washed with water. This material was dried over anhydrous potassium carbonate in vacuo to provide the title compound as a yellow crystalline solid (4.97 g), m.p. 109-112° C., which was used as such in the next step.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06900200B2 |
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| Quelldatensatz | uspto-grants-2005_05 |
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| ORD ID | ord-41d5697da93844aaa9123f1992552625 |
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| Quellennotiz | uspto-grants-2005_05 |
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