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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592992Generated: October 30, 2026

Potassium Iodide → 3-Iodo-5-(methoxycarbonyl)benzoic acid

https://huagongshe.com/reaction/1592992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant3-Amino-5-(methoxycarbonyl)benzoic acidHCID 13557643—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product3-Iodo-5-(methoxycarbonyl)benzoic acidHCID 1584039155.1%

Reaction Steps

To an ice-cold, stirred solution of commercially available 3-amino-5-(methoxycarbonyl)benzoic acid (5.19 g, 26.59 mmol) in 2 N hydrochloric acid (156 mL) was added a solution of sodium nitrite (1.84 g, 26.67 mmol) in water (10.8 mL). This mixture was then added dropwise to an ice-cold, stirred solution of potassium iodide (8.84 g, 53.25 mmol) in water (26.2 mL). After stirring for 35 min, the reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with 5% aqueous sodium thiosulfate, and saturated sodium chloride, dried (sodium sulfate), and concentrated under reduced pressure. Purification by flash column chromatography (silica, 50:50:2 hexanes/ethyl acetate/acetic acid) afforded the title compound (4.48 g, 55% yield) as an off-white solid. ESI-MS (m/z): 305 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07294642B2
Source datasetuspto-grants-2007_11
ORD IDord-f95ee87fc6c347dd90c872a903474685
Source noteuspto-grants-2007_11