Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931001Generated: October 25, 2026

N-Iodosuccinimide → 3-Bromo-2-iodo-5-(trifluoromethyl)aniline

https://huagongshe.com/reaction/931001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant3-Bromo-5-(trifluoromethyl)anilineHCID 2735880—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
Product3-Bromo-2-iodo-5-(trifluoromethyl)anilineHCID 5754614268.3%

Reaction Steps

To a solution of 3-bromo-5-(trifluoromethyl)aniline (5.00 g) in acetic acid (40 mL) was added N-iodosuccinimide (5.16 g) at 0° C., and the mixture was stirred overnight at room temperature under nitrogen atmosphere. The reaction mixture was diluted with ethyl acetate, washed with 10% aqueous sodium thiosulfate solution, saturated aqueous sodium bicarbonate solution and saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (5.21 g). 1H NMR (300 MHz, CDCl3) δ 4.58 (2H, brs), 6.84 (1H, d, J=1.1 Hz), 7.23 (1H, d, J=1.1 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296746B2
Source datasetuspto-grants-2016_03
ORD IDord-4742f0dfcf32470bad86ff75ea01a13b
Source noteuspto-grants-2016_03