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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-FluoronitrobenzeneHCID 9590—
EduktPotassium CarbonateHCID 11430—
EduktHCID 178418800HCID 178418800—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-(4-Methyl-1h-imidazol-1-yl)benzenamineHCID 1600517060%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889706B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-00dfce051fc5487cb5574f6d0be9d388
Quellennotizuspto-grants-2014_11