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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096193Generated: October 27, 2026

Potassium Iodide → 2-Chloro-4-iodo-1-trifluoromethylbenzene

https://huagongshe.com/reaction/1096193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantSodium ThiosulfateHCID 24477—
Reactant3-Chloro-4-(trifluoromethyl)anilineHCID 67962—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product2-Chloro-4-iodo-1-trifluoromethylbenzeneHCID 6678321273.4%

Reaction Steps

To a solution of 3-chloro-4-(trifluoromethyl)aniline (450 mg, 2.30 mmol) and toluene 4-sulfonic acid (1.19 g, 6.92 mmol) in CH3CN (10 mL) was added a solution of potassium iodide (955 mg, 5.76 mmol) and sodium nitrite (318 mg, 4.61 mmol) in water (1.8 mL) over 15 min at 10° C., then after 20 min the reaction mixture was poured onto water, neutralized with sat. aq. NaHCO3 solution, treated with 2 M aq. sodium thiosulfate solution (6 mL), and extracted with EtOAc. The organic layer was dried (MgSO4), filtered, and evaporated to afford the title compound (517 mg) as a light brown oil, which was directly used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138175B2
Source datasetuspto-grants-2012_03
ORD IDord-7ef7172636944e12b9986b5fd24a4f94
Source noteuspto-grants-2012_03