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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1242972Erstellt: 25. Oktober 2026

Indole → 1-(2-Methoxyphenyl)-1H-indole

https://huagongshe.com/reaction/1242972

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIndoleHCID 798—
Edukto-IodoanisoleHCID 68257—
Produkt1-(2-Methoxyphenyl)-1H-indoleHCID 2827514100%

Reaktionsschritte

Using general procedure A, indole (146 mg, 1.25 mmol)) was coupled with 2-iodoanisole (135 μL, 1.04 mmol). The crude product was purified by flash chromatography on silica gel (2×15 cm; hexane-ether 15:1; 15 mL fractions). Fractions 6–10 provided 232 mg (100% yield) of the product as a colorless oil. The 1H NMR spectrum was in accord with that reported by Maiorana et al. Maiorana, S.; Baldoli, C.; Del Buttero, P.; Di Ciolo, M.; Papagni, A. Synthesis 1998, 735.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07115784B2
Quelldatensatzuspto-grants-2006_10
ORD IDord-f4050f1d06cb4e53a9f80bac8e211b54
Quellennotizuspto-grants-2006_10