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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 240960Erstellt: 24. Oktober 2026

Ethyl Acetate → 3,5,6-trifluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine

https://huagongshe.com/de/reaction/240960

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktAmmonium ChlorideHCID 25517—
Edukt2,3,5-trifluoro-N-(2-fluoro-4-iodophenyl)-6-nitroanilineHCID 57430072—
KatalysatorIronHCID 23925—
LösungsmittelEthanolHCID 702—
Produkt3,5,6-trifluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamineHCID 5938634366,4%

Reaktionsschritte

To the stirred solution of (2-fluoro-4-iodo-phenyl)-(2,3,5-trifluoro-6-nitro-phenyl)-amine 3 (5.2 gm, 12.62 mmol) in EtOH (200 ml), ammonium chloride (10.12 gm, 189.3 mmol) and iron powder (10.57 gm, 189.3 mmol) was added. This reaction mixture was kept stirring at reflux for 16 hours. Reaction mixture was allowed to cool and was filtered over celite and concentrated to dryness. The residue obtained was taken into EtOAc and was washed with water. The EtOAc layer was dried over sodium sulfate and further purified by crystallization from EtOH to provide off-white solid (3.2 gm, yield: 66.39%). M−H+: 381.1. 1H NMR (DMSO, 300 MHz): 5.0 (s, 2H); 6.2 (t, 1H); 7.2-7.3 (m, 2H); 7.45 (s, 1H); 7.5 (d, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08648116B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-600e11873279499c841ab360c962f1a4
Quellennotizuspto-grants-2014_02