Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1297353Erstellt: 26. Oktober 2026

Methyl iodide → Methyl 1-methyl-1H-indole-3-carboxylate

https://huagongshe.com/reaction/1297353

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktSodium hydrideHCID 24758—
EduktMethyl indole-3-carboxylateHCID 589098—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
ProduktMethyl 1-methyl-1H-indole-3-carboxylateHCID 84200696,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

NaH (60% dispersion in mineral oil, 8.56 g, 214.0 mmole) was added portionwise, allowing for gas evolution, to a solution of methyl 1H-indole-3-carboxylate (25.00 g, 142.7 mmole) in DMF (350 mL) at 0° C. When the NaH addition was complete, methyl iodide (44.4 mL, 713.5 mmole) was added at 0° C. The reaction was stirred at 0° C. for 15 minutes then at RT overnight. The reaction was diluted with water and extracted with ethyl acetate. The combined extracts were dried over K2CO3 and concentrated to afford the title compound (26.00 g, 96%) as an orange solid: MS (ES) m/e 190 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07250424B2
Quelldatensatzuspto-grants-2007_07
ORD IDord-57bb5209b7f64520afe125b22fee0872
Quellennotizuspto-grants-2007_07