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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1791469Erstellt: 26. Oktober 2026

Ethanol → ethyl {1-benzyl-5-phenyl-1H-indol-3-yl}(oxo)acetate

https://huagongshe.com/reaction/1791469

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktOxalyl chlorideHCID 65578—
Edukt1-Benzyl-5-phenyl-1H-indoleHCID 22032937—
Produktethyl {1-benzyl-5-phenyl-1H-indol-3-yl}(oxo)acetateHCID 2203297866%

Reaktionsschritte

Ethyl {1-benzyl-5-phenyl-1H-indol-3-yl}(oxo)acetate was prepared from 1-benzyl-5-phenyl-1H-indole (0.846 g, 2.99 mmol), oxalyl chloride (0.78 mL, 9.0 mmol), and ethanol (2 mL), following the procedure described in Step 3 of Example 1. Purification by flash chromatography (Biotage apparatus) using 5-7.5% ethyl acetate in hexane as an eluant yielded the title compound as a light yellow solid (0.754 g, 66%), mp: 116-117° C. Mass spectrum (+ES, [M+H]+) m/z 384; 1HNMR (500 MHz, DMSO-d6): δ 8.7 (s, 1H), 8.4 (d, 1H, J=0.92 Hz), 7.6-7.7 (m, 3H), 7.55-7.6 (m, 1H), 7.45 (t, 2H, J=7.7 Hz), 7.3-7.4 (m, 6H), 5.65 (s, 2H), 4.35 (q, 2H, J=7.1 Hz), and 1.35 ppm (t, 3H, J=7.1 Hz).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07074817B2
Quelldatensatzuspto-grants-2006_07
ORD IDord-137b44c12907427ba89083a530a22b08
Quellennotizuspto-grants-2006_07