Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 39196Erstellt: 24. Oktober 2026

Stannous chloride dihydrate → 5-Bromo-2-fluoro-4-methylaniline

https://huagongshe.com/de/reaction/39196

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktStannous chloride dihydrateHCID 61436—
EduktSodium BicarbonateHCID 516892—
Edukt1-Bromo-4-fluoro-2-methyl-5-nitrobenzeneHCID 10036983—
LösungsmittelEthanolHCID 702—
Produkt5-Bromo-2-fluoro-4-methylanilineHCID 4673911431,9%

Reaktionsschritte

To a stirred solution of 1-bromo-4-fluoro-2-methyl-5-nitrobenzene (18.0 g) in ethanol (300 mL) was added SnCl2.2H2O (51.8 g, 0.230 mol) at room temperature. The mixture was heated at reflux for 3 h. The solvent was evaporated under reduced pressure to give a residue, which was poured into ice water. The aqueous phase was basified with sat. NaHCO3 to pH 7. The solid was filtered off and the filtrate was extracted with dichloromethane (200 mL×3). The combined organics were dried over anhydrous Na2SO4 and evaporated under reduced pressure. The residue was purified by column chromatography (petroleum ether/EtOAc=10/1) to afford 5-bromo-2-fluoro-4-methylaniline (5.0 g, 30% yield for two steps). 1NMR (400 MHz, CDCl3) δ 6.96 (d, J=8.8 Hz, 1H), 6.86 (d, J=11.6 Hz, 1H), 3.64 (br, 2H), 2.26 (s, 3H). MS (ESI) m/z (M+H+) 204.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524767B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-4faec5fa3e7a4b489140c41b8b82cf54
Quellennotizuspto-grants-2013_09