Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471458Generated: November 3, 2026

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

https://huagongshe.com/reaction/471458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
ReactantPotassium IodideHCID 4875—
ReactantSodium SulfiteHCID 24437—
Reactant2-Bromo-3-(trifluoromethyl)anilineHCID 94058—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product2-Bromo-1-iodo-3-(trifluoromethyl)benzeneHCID 5348447085.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Bromo-3-trifluoromethylaniline (8 g, 33.33 mmol) is suspended in water (90 mL) and cooled to 0° C. 96% H2SO4 (26.7 mL, 13.7 mmol) is added and the mixture stirred for 30 minutes. NaNO2 (2.41 g, 35 mmol) is dissolved in a small quantity of water and added dropwise at 0° C. The mixture is stirred for 30 minutes then potassium iodide (9.24 g, 55.66 mmol) and iodine (9.31 g, 36.66 mmol) in water are added dropwise with cooling. The mixture is stirred until gas evolution ceases then warmed to 40° C. and allowed to cool to room temperature. The mixture is shaken with excess aqueous Na2SO3 solution and extracted with ethyl acetate. The organic extracts are evaporated and the residue purified by flash chromatography (eluent: cyclohexane) to give the title compound (Yield 10.0 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633182B2
Source datasetuspto-grants-2014_01
ORD IDord-a6e6edc46afe4276bf509ccdc0aa1228
Source noteuspto-grants-2014_01