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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435661Generated: October 30, 2026

Hydrochloric Acid → 2-Iodo-5-methylbenzoic acid

https://huagongshe.com/reaction/435661

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 Conditions

Temperature0 °C

Reaction Steps

20 g of 5-methyl-anthranilic acid are suspended in 200 ml of 3-N hydrochloric acid at 0° C. There is added dropwise thereto with stirring a solution of 10 g of sodium nitrite and 20 ml of water and the mixture is 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 then stirred for a further 30 minutes at room temperature and for 2 hours under reflux. The mixture is then cooled, sodium thiosulphate is added until the solution is yellow (5 g) and the crystalline 2-iodo-5-methyl-benzoic acid obtained is filtered under suction and washed with water until neutral. The crude acid is dissolved in ether, washed well with sodium thiosulphate solution and water, dried over sodium sulphate and evaporated. There are obtained light-brown crystals of melting point 100°-112° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04006144
Source datasetuspto-grants-1977_02
ORD IDord-5ec3964d607c41b4a54e23b8286ab8b7
Source noteuspto-grants-1977_02