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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541294Generated: November 3, 2026

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

https://huagongshe.com/reaction/541294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
Reactant4-Chloro-2-methylbenzoic acidHCID 348269—
SolventAcetic AcidHCID 176—
Product4-Chloro-5-iodo-2-methylbenzoic acidHCID 68288948—

Reaction Conditions

Temperature110 °C

Reaction Steps

To a round-bottom flask was added a solution of 4-chloro-2-methylbenzoic acid (30.0 g, 176 mmol, 1.00 equiv) in acetic acid (300 mL). NaIO4 (19.0 g, 88.8 mmol, 0.50 equiv), I2 (49.0 g, 193 mmol, 1.10 equiv), and sulfuric acid (3 mL) were added to the reaction. The resulting mixture was stirred overnight at 110° C. After cooling to ambient temperature, the reaction was carefully quenched with 500 mL of Na2S2O3 (aq., sat.). The resulting solids were collected by filtration and then dissolved in 500 mL of ethyl acetate. The organic phase was washed with 2×200 mL of brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. This resulted in 20.0 g (38%) of 4-chloro-5-iodo-2-methylbenzoic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871790B2
Source datasetuspto-grants-2014_10
ORD IDord-6accd657c61143f78d8345e0113e9818
Source noteuspto-grants-2014_10