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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7496Erstellt: 24. Oktober 2026

5-Benzyloxy-2-fluoro-4-methylnitrobenzene → 5-Benzyloxy-2-fluoro-4-methylaniline

https://huagongshe.com/de/reaction/7496

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-Benzyloxy-2-fluoro-4-methylnitrobenzeneHCID 21991057—
KatalysatorIronHCID 23925—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
Produkt5-Benzyloxy-2-fluoro-4-methylanilineHCID 2199106887,7%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

The starting material, 5-benzyloxy-2-fluoro-4-methylaniline, was obtained by adding iron powder (2.88 g, 51 mmol), in portions, to a solution of 5-benzyloxy-2-fluoro-4-methylnitrobenzene (4.8 g, 18 mmol) in acetic acid (33 ml) and water (5.7 ml), at ambient temperature. The mixture was heated and after stirring at 100° C. for 10 minutes, it was cooled and partitioned between ethyl acetate and water. The organic layer was washed with water, aqueous saturated sodium carbonate solution and then brine, dried (MgSO4) and the solvent evaporated. The residue was purified by flash chromatography using petroleum ether/ethyl acetate (8/2) as eluent to give 5-benzyloxy-2-fluoro-4-methylaniline (3.65 g, 87%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087602B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-c8db631387344b1d934a549994ef9606
Quellennotizuspto-grants-2006_08