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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 9551Erstellt: 24. Oktober 2026

Formic Acid → N-(2-fluoro-4-iodophenyl)formamide

https://huagongshe.com/de/reaction/9551

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormic AcidHCID 284—
EduktAcetic AnhydrideHCID 7918—
Edukt2-Fluoro-4-iodoanilineHCID 185694—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelTolueneHCID 1140—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
ProduktN-(2-fluoro-4-iodophenyl)formamideHCID 2354934197,1%

Reaktionsschritte

To a cooled solution (0° C.) of 4-iodo-2 fluoroaniline (3.05 g, 12.9 mmol) in tetrahydrofuran (15 mL) and toluene (15 mL), was slowly added a mixture of acetic anhydride (1.39 mL, 14.7 mmol) and formic acid (0.83 mL, 22.0 mmol). The reaction mixture was stirred at rt overnight, then diluted with ethyl acetate (100 mL) and 1N aqueous HCl (100 mL). The layers were separated, and the organic layer was washed with water and saturated sodium carbonate solution, and dried over sodium sulfate. The solvent was removed under reduced pressure to afford 2-fluoro-4-iodophenylformamide as an off-white solid (3.32 g, 97%). GC-MS ret. time 2.27 min, m/z 265 (M+); 1H NMR (300 MHz, CDCl3) δ: 7.37–7.51 (m, 3H), 8.13 (t, 1H), 8.46 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091228B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-5371b54496fc4e8fb22218bcae433455
Quellennotizuspto-grants-2006_08