HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 378899Erstellt: 25. Oktober 2026
4-Methoxybenzenecarboximidamide → 2-(4-Methoxyphenyl)-4-(2-nitrophenyl)imidazole
https://huagongshe.com/reaction/378899
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Methoxybenzenecarboximidamide | HCID 229074 | — |
| Edukt | 2-Bromo-2'-nitroacetophenone | HCID 244025 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 2-(4-Methoxyphenyl)-4-(2-nitrophenyl)imidazole | HCID 178488923 | 78,1% |
Reaktionsschritte
A mixture of 2-bromo-2′-nitroacetophenone (18 g), 4-methoxybenzamidine (20 g), and silica gel (20 g) in acetonitrile (500 ml) is heated at 40° C. for 24 hours. The reaction is evaporated and the residue put on a layer of silica gel and eluted with 50% ethyl acetate/hexane (1500 ml). The solution is evaporated under reduced pressure to approximately 250 ml and extracted with 5% HCl (3×250 ml). The combined aqueous solution is basified with K2CO3 and extracted with ethyl acetate (3×400 ml) to afford 2-(4-methoxyphenyl)-4-(2-nitrophenyl)-imidazole (17 g) as a dark yellow oil which is used in the next step without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06297252B1 |
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| Quelldatensatz | uspto-grants-2001_10 |
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| ORD ID | ord-ad59b6e86cc441af88a72d2c9740d441 |
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| Quellennotiz | uspto-grants-2001_10 |
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