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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866589Generated: October 30, 2026

Hydrochloric Acid → 2-Iodo-5-methylbenzoic acid

https://huagongshe.com/reaction/866589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium IodideHCID 4875—
ReactantSodium ThiosulfateHCID 24477—
Reactant2-Amino-5-methylbenzoic acidHCID 76255—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product2-Iodo-5-methylbenzoic acidHCID 142941—

Reaction Steps

20 G. of 5-methyl-anthranilic acid are suspended in 200 ml. of 3-N hydrochloric acid at 0° C. A solution of 10 g. of sodium nitrite and 20 ml. of water is added dropwise thereto with stirring and the mixture is further stirred for 25 minutes at 0° C. A solution of 26.5 g. of potassium iodide, 30 ml. of 3-N hydrochloric acid and 30 ml. of water is then added dropwise at 5°-10° C. The mixture is stirred for an additional 30 minutes at room temperature and for 2 hours at reflux. The mixture is cooled and sodium thiosulfate is added until the solution is yellow (5 g.). The crystalline 2-iodo-5-methyl-benzoic acid obtained is removed by filtration under vacuum and washed neutral with water. The crude acid is dissolved in ether, washed well with sodium thiosulfate solution and water, dried over sodium sulfate and evaporated, and there are obtained light-brown crystals having a melting point of 100°-112° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04100173
Source datasetuspto-grants-1978_07
ORD IDord-d37962cbeded487d8225d8cd73f92376
Source noteuspto-grants-1978_07