Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1167488Erstellt: 25. Oktober 2026

Ammonium formate → 3-Fluoro-4-(4-methyl-1H-imidazol-1-yl)aniline

https://huagongshe.com/reaction/1167488

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium formateHCID 2723923—
Edukt1-(2-fluoro-4-nitrophenyl)-4-methyl-1H-imidazoleHCID 21876596—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Fluoro-4-(4-methyl-1H-imidazol-1-yl)anilineHCID 2187663890,5%

Reaktionsschritte

3-Fluoro4-(4-methyl-imidazol-1-yl)nitrobenzene (64.7 g, 0.293 M) was dissolved in a mixture of MeOH (200 ml) and tetrahydrofuran (800 ml), cooled to 0° under nitrogen, and treated with ammonium formate (99.3 g, 1.46 M) followed by palladium on charcoal (10%. 2.5 g). The mixture was stirred at ambient temperature for 48 hours, filtered through celite, celite washed with MeOH (200 ml), and filtrate evaporated to dryness. The residue was partitioned between EtOAc (800 ml) and 10% aqueous sodium bicarbonate (250 ml). The organic layer was separated, washed with brine (250 ml), dried (magnesium sulfate) and evaporated to give title compound (50.6 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06617339B1
Quelldatensatzuspto-grants-2003_09
ORD IDord-4fe3fbdddf794d7ba7c0bca1f7ba7191
Quellennotizuspto-grants-2003_09