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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 8114Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/8114

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-difluoroindole (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
PatentnummerUS07087635B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-563d6e04fa2144da9e95cdda593c8abd
Quellennotizuspto-grants-2006_08