Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2426847Erstellt: 26. Oktober 2026

Iodine → 3-iodo-5,6-dimethoxy-1-methyl-1H-indole

https://huagongshe.com/reaction/2426847

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktDimethylformamideHCID 6228—
EduktMethyl iodideHCID 6328—
EduktPotassium HydroxideHCID 14797—
EduktSodium ThiosulfateHCID 24477—
Edukt5,6-DimethoxyindoleHCID 84431—
LösungsmittelWaterHCID 962—
Produkt3-iodo-5,6-dimethoxy-1-methyl-1H-indoleHCID 67147447—

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

0.465 g of powdered potassium hydroxide is added to a solution of 0.5 g of 5,6-dimethoxy-1H-indole in 15 ml of dimethylformamide. A solution of 0.725 g of bisublimated iodine in 15 ml of dimethylformamide is added dropwise to the above mixture. After agitation of the reaction medium for approximately 3 hours at a temperature in the region of 20° C., 0.21 ml of iodomethane is added dropwise, maintaining the mixture at this same temperature by cooling using a water bath. After agitation at around 20° C. for 1 hour 30 minutes, the mixture is run into a solution of 1.5 g of sodium thiosulfate in 150 ml of water cooled to around 5° C., and agitated for approximately 10 minutes. The precipitate is filter-dried, washed with five times 5 ml of water cooled to around 5° C., and then dried under vacuum (13 kPa) over phosphorus pentaoxide. 0.78 g of 3-iodo-5,6-dimethoxy-1-methyl-1H-indole is obtained in the form of a solid, the characteristics of which are as follows:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07968566B2
Quelldatensatzuspto-grants-2011_06
ORD IDord-d8b6e25a6b8e41cba01926c0db395b78
Quellennotizuspto-grants-2011_06