Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217283Generated: October 25, 2026

Iodine → 2,4-Dichloro-5-iodobenzoic acid

https://huagongshe.com/reaction/217283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant2,4-Dichlorobenzoic AcidHCID 5787—
ReactantSodium IodateHCID 23675764—
SolventSulfuric AcidHCID 1118—
Product2,4-Dichloro-5-iodobenzoic acidHCID 68417909121.2%

Reaction Steps

Sodium iodate (4.4 g) and iodine (11.1 g) were added to 90% sulfuric acid (330 mL), and stirred at room temperature for 8 hours. 2,4-Dichlorobenzoic acid (21 g) commercially available was added and stirred at the same temperature for 24 hours. The reaction solution was poured into ice water (3 L), and the precipitated solid material was collected by filtration. Further, the solid material was washed with water, and dried under reduced pressure. 2,4-Dichloro-5-iodobenzoic acid (16.8 g) was obtained by recrystallization (acetic acid-water). The resulting 2,4-dichloro-5-iodobenzoic acid (2 g) was dissolved in a mixture of dichloromethane (20 mL) and methanol (20 mL). Trimethylsilyldiazomethane (hexane solution, 2 M) was added dropwise until the solution became yellow. A small amount of acetic acid was added, and then the resulting mixture was concentrated under reduced pressure. The resulting residue was recrystallized using hexane to give the title compound 2,4-dichloro-5-iodobenzoic acid methyl ester as white solid (2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193351B2
Source datasetuspto-grants-2012_06
ORD IDord-462cf85cee2c4c528734f47e9d42eaf1
Source noteuspto-grants-2012_06