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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497582Generated: October 30, 2026

Dichloromethane → 2-Amino-4-fluoro-5-iodobenzoic acid

https://huagongshe.com/reaction/1497582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Fluoroanthranilic acidHCID 2724967—
ReactantTrimethylbenzylammonium DichloroiodateHCID 56924451—
SolventMethanolHCID 887—
Product2-Amino-4-fluoro-5-iodobenzoic acidHCID 2195214677%

Reaction Steps

To a vigorously stirred solution of dichloromethane (700 ml), methanol (320 ml), and 2-amino-4-fluoro-benzoic acid (33.35 grams, 215 mmoles) was added solid sodium hydrogencarbonate (110 grams, 1.31 moles) followed by portion addition of benzyltrimethyl ammonium dichloroiodate (82.5 grams, 237 mmoles). The mixture was allowed to stir for 48 hours. The mixture was filtered to remove the insolubles. The remaining solid residue was washed with 200 ml of dichloromethane. The filtrate was concentrated and redissolved in a one to one mixture of ethyl acetate (1 liter) and a 0.2 N solution of sodium hydroxide (1 liter), added to a 2 liter separatory funnel and extracted. The organic layer was washed with an additional 200 ml of water. The aqueous layers were combined and acidified with 2N hydrochloric acid. The resulting precipitate was collected by suction filtration, washed with water and dried under vacuum at 60° C. to yield 46.5 grams (77%) of the title compound. 1H NMR (400 MHz, DMSO-d6) δ: 8.04 (d, 1H), 7.1 (s, broad, 2H), 6.63 (d, 1H). ESI-MS m/z 280 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199973B2
Source datasetuspto-grants-2015_12
ORD IDord-7e142ae5579e479f96cc96e219da3513
Source noteuspto-grants-2015_12