HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 336885Erstellt: 24. Oktober 2026
p-Fluoronitrobenzene → 4-(4-Methyl-1h-imidazol-1-yl)benzenamine
https://huagongshe.com/de/reaction/336885
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | p-Fluoronitrobenzene | HCID 9590 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | HCID 178418800 | HCID 178418800 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-(4-Methyl-1h-imidazol-1-yl)benzenamine | HCID 16005170 | 60% |
Reaktionsschritte
To a solution of compound 6.0 4-methyl imidazole (1 mL, 10 mmol, 1 equiv.) in DMF at room temperature was added 1-fluoro-4-nitrobenzene 6.1 (820 mg, 10 mmol, 1 equiv.) and K2CO3 (1.38 g, 10 mmol, 1 equiv.). The resulting mixture was heated to 110° c for 4h before being cooled to room temperature, filtered through celite, and washed with EtOAc (20 mL×4). The collected filtrate was further washed with brine (50 mL×3) and dried over Na2SO4. After removal of solvent, the residue was diluted with MeOH (20 mL). Pd/C (50 mg, 5% mass equiv.) was added and the reaction flask was charged with a H2 balloon and stirred overnight at room temperature. The mixture was filtered through celite and washed with EtOAc (20 mL×3). The collected filtrate was concentrated and the residue was purified via flash chromatography (hexanes:EtOAc=1:1) to afford the desired product 6.3 4-(4-methyl-1H-imidazol-1-yl)benzenamine (1.0 g; 60%). LC-MS (M+H):174.15
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08889706B2 |
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| Quelldatensatz | uspto-grants-2014_11 |
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| ORD ID | ord-00dfce051fc5487cb5574f6d0be9d388 |
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| Quellennotiz | uspto-grants-2014_11 |
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