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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427332Generated: November 3, 2026

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

https://huagongshe.com/reaction/2427332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantAcetic AnhydrideHCID 7918—
Reactant2-Fluoro-4-iodoanilineHCID 185694—
SolventHydrochloric AcidHCID 313—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductN-(2-fluoro-4-iodophenyl)formamideHCID 2354934197.1%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968576B2
Source datasetuspto-grants-2011_06
ORD IDord-cd11e9e96f9d4283be4a0275faf835bb
Source noteuspto-grants-2011_06