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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 565678Erstellt: 24. Oktober 2026

Indole → 1-Phenyl-1H-indole

https://huagongshe.com/de/reaction/565678

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIndoleHCID 798—
EduktPotassium BicarbonateHCID 516893—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelBromobenzeneHCID 7961—
Produkt1-Phenyl-1H-indoleHCID 182029124,2%

Reaktionsschritte

A suspension of indole (8.2 g), potassium bicarbonate (12 g) and copper (I) iodide (2.7 g) in bromobenzene (70 mL) was refluxed for 3 hours under nitrogen atmosphere. To the mixture copper (I) iodide (11 g) was added and the mixture was refluxed for additional 6 hours. The insoluble material was removed by filtration and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=50:1 to 20:1) to provide 8.4 g of the title compound. Yield 62%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06172085B2
Quelldatensatzuspto-grants-2001_01
ORD IDord-df943a1910d34487b1cad511b5518662
Quellennotizuspto-grants-2001_01