Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349080Generated: October 30, 2026

Hydrochloric Acid → 3-Iodo-5-(methoxycarbonyl)benzoic acid

https://huagongshe.com/reaction/349080

Reaction equation

Participants

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

Reaction Steps

To an ice-cold, stirred solution of 3-amino-5-(methoxycarbonyl)benzoic acid (5.19 g, 26.59 mmol) in a 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 3-iodo-5-(methoxycarbonyl)benzoic acid (4.48 g): 1H NMR (500 MHz, DMSO-d6): δ 13.49 (br s, 1H), 8.45–8.38 (m, 3H), 3.83 (s, 3H); ESI-MS (m/z): 305 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176242B2
Source datasetuspto-grants-2007_02
ORD IDord-238460582c0949ba9855193268a5ecf1
Source noteuspto-grants-2007_02