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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1623535Erstellt: 26. Oktober 2026

Methyl iodide → 4-Methoxy-1-methylindole

https://huagongshe.com/reaction/1623535

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktSodium hydrideHCID 24758—
Edukt4-Methoxy-1H-indoleHCID 138363—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-Methoxy-1-methylindoleHCID 595238—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 4-methoxy-1H-indole (CAS#4837-90-5, 4.0 g, 27.2 mmol) in THF (100 ml) at 0° C. was added sodium hydride (60% dispersion in oil, 1.63 g, 40.08 mmol). The reaction was stirred for 15 minutes at 0° C. and then put at room temperature for 1 h. The reaction was then re-cooled to 0° C. and iodomethane (2.209 ml, 35.3 mmol) was added. The reaction was then put at room temperature and permitted to stir for 45 minutes. The reaction was then quenched with saturated aqueous ammonium chloride and concentrated to approximately half of its original volume. Next, the reaction mixture was diluted with water and dichloromethane and the layers were separated. The aqueous layer was then extracted two additional times with dichloromethane. The organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated. The resulting residue was purified by silica gel flash chromatography (ethyl acetate-heptane 0 to 30%) to afford 4-methoxy-1-methyl-1H-indole; MS: (ES+) m/z 162.0 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08778972B2
Quelldatensatzuspto-grants-2014_07
ORD IDord-d1f78c374c5044569f7c89fa4d8614f4
Quellennotizuspto-grants-2014_07