HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 472160Erstellt: 25. Oktober 2026
Potassium Hydroxide → 4-(4-Methyl-1h-imidazol-1-yl)benzenamine
https://huagongshe.com/reaction/472160
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | Stannous chloride dihydrate | HCID 61436 | — |
| Edukt | 4-Methyl-1-(4-nitrophenyl)-1H-imidazole | HCID 16005169 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 4-(4-Methyl-1h-imidazol-1-yl)benzenamine | HCID 16005170 | 10.152,9% |
Reaktionsschritte
4-(4-methyl-1H-imidazol-1-yl)nitrobenzene (22.5 g; 0.87 mmol) is dissolved in abs. ethanol (250 mL), then SnCl2.2H2O (125 g; 0.55 mol) is added portion-wise, on cooling at 0° C. The resulting mixture is stirred at r.t. for 2 hours and heated at reflux overnight. The reaction mixture is then cooled at r.t. and the pH is adjusted to 12, by adding 30% KOH (500 mL), then KOH pellets under stirring. The resulting suspension is filtered and the cake is washed with ethanol, the combined filtrate and washings are concentrated and the residue is extracted with DCM. Concentration of the combined organic extracts afforded the title product as a slight brown solid (15.3 g; 80%), m.p.: 122-125° C. C10H11N3, MW 173.22.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08633208B2 |
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| Quelldatensatz | uspto-grants-2014_01 |
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| ORD ID | ord-38007aa131cc43e6ac40724e0553f5da |
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| Quellennotiz | uspto-grants-2014_01 |
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