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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552675Generated: October 31, 2026

Potassium Iodide → 1-Chloro-2-fluoro-5-iodo-3-(trifluoromethyl)benzene

https://huagongshe.com/reaction/552675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium NitriteHCID 23668193—
Reactant3-Chloro-4-fluoro-5-(trifluoromethyl)anilineHCID 29934847—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product1-Chloro-2-fluoro-5-iodo-3-(trifluoromethyl)benzeneHCID 6657071544.4%

Reaction Steps

In 300 mL of 6N hydrochloric acid, 4.00 g of 3-chloro-4-fluoro-5-trifluoromethylaniline was added, and stirred at room temperature for 30 minutes. In the mixture, a solution of 1.42 g of sodium nitrite in 5 mL of water was added dropwise at such a rate that internal temperature would not exceed 5° C. After the completion of the addition dropwise, it was continued to stir at the same temperature further for 1 hour. In the reaction mixture, a solution of 4.70 g of potassium iodide in 15 mL of water was added dropwise at the same temperature with stirring. After the completion of the addition dropwise, it was continued to stir at the same temperature further for 1 hour and then at room temperature for 15 hours. After the completion of the reaction, the reaction mixture was extracted with 50 mL of diethyl ether twice. The combined organic phases were dehydrated with and dried over saturated sodium chloride aqueous solution and then anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure to obtain 2.70 g of the crude aimed product as yellow oily substance. The resulting product was used as such without purification for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951828B1
Source datasetuspto-grants-2011_05
ORD IDord-3e5f32adbd1b4c17b9760d524077f4f9
Source noteuspto-grants-2011_05