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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672891Generated: October 26, 2026

Hydrochloric Acid → 2,4-Difluoro-6-((2-fluoro-4-iodophenyl)amino)benzoic acid

https://huagongshe.com/reaction/1672891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium amideHCID 24532—
Reactant2-Fluoro-4-iodoanilineHCID 185694—
Reactant2,4,6-Trifluorobenzoic acidHCID 520373—
SolventAcetonitrileHCID 6342—
Product2,4-Difluoro-6-((2-fluoro-4-iodophenyl)amino)benzoic acidHCID 6705156059.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

2,4,6-Trifluorobenzoic acid (643 mg, 3.65 mmol) and 2-fluoro-4-iodoaniline (1.0 g, 4.22 mmol) were taken into acetonitrile (30 mL) followed by addition of lithium amide (290 mg, 12.7 mmol) and the mixture was heated to 60° C. under a nitrogen atmosphere for one hour. On cooling to room temperature the mixture was added to 1 N aqueous hydrochloric acid (100 mL) and the precipitate formed was collected by filtration and washed once with water then hexanes and dried in vacuo to give 2,4-difluoro-6-[(2-fluoro-4-iodophenyl)amino]benzoic acid (849 mg, 59% yield) as a tan solid. 1H-NMR (400 MHz, D6-DMSO): 13.72 (br s, 1H), 9.46 (s, 1H), 7.75 (d, 1H), 7.56 (d, 1H) 7.28 (tr, 1H), 6.73-6.67 (m, 1H), 6.53 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07999006B2
Source datasetuspto-grants-2011_08
ORD IDord-71eed6c18d0749c3ba03857472705f2d
Source noteuspto-grants-2011_08