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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406508Generated: October 30, 2026

Iodine → 2-Bromo-1-iodo-3-(trifluoromethyl)benzene

https://huagongshe.com/reaction/2406508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
ReactantSodium SulfiteHCID 24437—
Reactant2-Bromo-3-(trifluoromethyl)anilineHCID 94058—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product2-Bromo-1-iodo-3-(trifluoromethyl)benzeneHCID 53484470—

Reaction Conditions

Temperature40 °C

Reaction Steps

An ice-cold solution of NaNO2 (0.15 g) in water (0.5 mL) is added to a mixture of 2-bromo-3-trifluoromethyl-aniline (0.48 g), concentrated H2SO4 (2 mL), and water (1.8 mL) at ca. 5° C. The mixture is stirred in the cooling bath for 20 min and then poured into a solution of KI (0.56 g) and I2 (0.56 g) in water (0.5 mL). After ceasing of gas evolution, the mixture is heated to 40° C. and stirred at this temperature for 1 h. The mixture is cooled to room temperature and aqueous Na2SO3 solution is added. The resulting mixture is extracted with ethyl acetate and the combined extracts are dried (Na2SO4) and concentrated. The solvent is evaporated and the residue is chromatographed (cyclohexane/ethyl acetate 95:5→90:10) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809376B2
Source datasetuspto-grants-2014_08
ORD IDord-86e84dcf4bc8443c92ce3466c3e55e1a
Source noteuspto-grants-2014_08