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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1272235Erstellt: 26. Oktober 2026

Dichloromethane → 5,7-Difluoro-3-iodo-1-(phenylsulfonyl)-1H-indole

https://huagongshe.com/reaction/1272235

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktBenzenesulfonyl chlorideHCID 7369—
EduktIodine chlorideHCID 24640—
Edukt5,7-difluoro-1H-indoleHCID 2778730—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelPyridineHCID 1049—
LösungsmittelTolueneHCID 1140—
LösungsmittelSodium HydroxideHCID 14798—
Produkt5,7-Difluoro-3-iodo-1-(phenylsulfonyl)-1H-indoleHCID 2201478487%

Reaktionsschritte

The 1.0 M ICl in CH2Cl2 (43 ml, 43 mmol) is added to a solution of 5,7-difluoro-indole (6 g, 39 mmol) in 35 ml pyridine under N2 at 0° C. and the resulting mixture is stirred for 30 minutes. The reaction is diluted with toluene and washed with brine, 1N HCl, 1N NaOH, dried (Na2SO4), filtered and concentrated. The crude 3-iodo-5,7-difluoroindole is stirred in toluene (85 ml) and 5 N NaOH (70 ml), tetrabutylammonium bromide (1.25 g, 3.9 mmol), then benzenesulfonyl chloride (6.2 ml, 48 mmol) are added and the resulting mixture is stirred 24 hours. The two phase reaction mixture is diluted with toluene, washed with brine, dried (Na2SO4), filtered, concentrated and the residue is triturated with diethyl ether/petroleum ether. The resulting solid is filtered to give 14.2 g of N-Benzenesulfonyl-3-iodo-5,7-difluoroindole (87%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07208505B2
Quelldatensatzuspto-grants-2007_04
ORD IDord-940f13e358e24caa9cd489bc6fd36e80
Quellennotizuspto-grants-2007_04