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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2360488Erstellt: 24. Oktober 2026

Methyl iodide → 7-bromo-1-methyl-1H-indole-2-carboxylic acid

https://huagongshe.com/de/reaction/2360488

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktSodium HydroxideHCID 14798—
EduktSodium hydrideHCID 24758—
EduktEthyl 7-bromo-1H-indole-2-carboxylateHCID 7017885—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt7-bromo-1-methyl-1H-indole-2-carboxylic acidHCID 58493996—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

7.37 g ethyl 7-bromo-1H-indole-2-carboxylate are dissolved in 50 ml N,N-dimethylformamide, cooled to 0° C. and combined with 1.16 g sodium hydride (60% in mineral oil). The mixture is stirred for 20 minutes and then 1.78 ml methyl iodide are added dropwise. Then the mixture is allowed to come up to ambient temperature and stirred for 12 hours. Then 80 ml of methanol and 27.5 ml 2 N sodium hydroxide solution are added and the mixture is stirred for 3 hours at ambient temperature. The methanol is eliminated in vacuo, the residue is mixed with water and the precipitate is suction filtered. The filtrate is washed twice with ethyl acetate and the aqueous phase is combined with sufficient 2 N hydrochloric acid to give a pH of 2. The precipitated solid is suction filtered, washed with water and dried.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08686022B2
Quelldatensatzuspto-grants-2014_04
ORD IDord-8a97a9a8ac2e4c72bfde979aa9bcad87
Quellennotizuspto-grants-2014_04