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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215133Generated: October 31, 2026

Iodine → 5-Chloro-4-iodo-2-methoxybenzoic acid

https://huagongshe.com/reaction/2215133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPotassium IodideHCID 4875—
Reactant4-Amino-5-chloro-2-methoxybenzoic acidHCID 81626—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
Product5-Chloro-4-iodo-2-methoxybenzoic acidHCID 1679185859.6%

Reaction Steps

A stirred solution of 4-amino-5-chloro-2-methoxy benzoic acid (12.25 g , 60.8 mmol) in water (136 mL ) and concentrated sulfuric acid (34 mL) was cooled to 0° C. in a flask fitted with an overhead stirrer. A solution of sodium nitrite (4.62 g , 66.9 mmol) in water (26 mL) was added dropwise while keeping the internal temperature around 0° C. Potassium iodide (11.11 g , 66.9 mmol) and iodine (4.246 g , 33.5 mmol) were dissolved in water (130 mL) and added dropwise to the stirred reaction mixture. After 2 hours the reaction was extracted with ethyl acetate. The organic extracts were then washed with 10% sodium thiosulfate and brine, then dried over magnesium sulfate, filtered and evaporated to dryness to yield 11.32 g of the title compound, m.p. 150–151° C. This material was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109193B2
Source datasetuspto-grants-2006_09
ORD IDord-5f4f748665e04732b21f3bae4913b9e9
Source noteuspto-grants-2006_09