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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1072607Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/1072607

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
PatentnummerUS06911463B2
Quelldatensatzuspto-grants-2005_06
ORD IDord-c496902e20ac473d8baa4a21b4e14b25
Quellennotizuspto-grants-2005_06