Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 931001Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/931001

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-IodosuccinimideHCID 120273—
Edukt3-Bromo-5-(trifluoromethyl)anilineHCID 2735880—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelEthyl AcetateHCID 8857—
Produkt3-Bromo-2-iodo-5-(trifluoromethyl)anilineHCID 5754614268,3%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09296746B2
Quelldatensatzuspto-grants-2016_03
ORD IDord-4742f0dfcf32470bad86ff75ea01a13b
Quellennotizuspto-grants-2016_03