HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2041706Erstellt: 26. Oktober 2026
Ammonium formate → 4-(4-Methyl-1h-imidazol-1-yl)benzenamine
https://huagongshe.com/reaction/2041706
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ammonium formate | HCID 2723923 | — |
| Edukt | 4-Methyl-1-(4-nitrophenyl)-1H-imidazole | HCID 16005169 | — |
| Katalysator | Palladium | HCID 23938 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 4-(4-Methyl-1h-imidazol-1-yl)benzenamine | HCID 16005170 | 90% |
Reaktionsschritte
Ammonium formate (2.202 g, 34.9 mmol) and palladium (10% w/w on carbon, 50% wet, 0.473 g, 4.44 mmol) were added to a solution of 4-methyl-1-(4-nitrophenyl)-1H-imidazole (for a preparation see intermediate 93) (4.73 g, 23.28 mmol) in ethanol (150 mL) and the resulting mixture was refluxed under nitrogen for 1 h then cooled to room temperature. An extra portion of ammonium formate (2.202 g, 34.9 mmol) was then added and the resulting mixture was refluxed for a further hour then cooled to room temperature and filtered through celite. Most of the solvent was removed in vacuo and the residue was loaded on a 50 g SCX column which was eluted with MeOH (5 CV) then with 2N NH3 in MeOH (5 CV). The ammonia fractions were combined and concentrated in vacuo to give 4-(4-methyl-1H-imidazol-1-yl)aniline (3.92 g, 21.06 mmol, 90%) as a yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08580957B2 |
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| Quelldatensatz | uspto-grants-2013_11 |
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| ORD ID | ord-caddad1bf5fa4089bbea590acdfd991d |
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| Quellennotiz | uspto-grants-2013_11 |
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