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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 241619Erstellt: 25. Oktober 2026

Indole → 1-(4-methoxyphenyl)-3-(methylthio)-1H-indole

https://huagongshe.com/reaction/241619

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIndoleHCID 798—
EduktSodium HydroxideHCID 14798—
EduktMagnesium BromideHCID 82241—
Edukt1-(4-methoxyphenyl)-1H-indoleHCID 775715—
Edukt2-(Methylthio)isoindoline-1,3-dioneHCID 4101460—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelDimethylacetamideHCID 31374—
Produkt1-(4-methoxyphenyl)-3-(methylthio)-1H-indoleHCID 5837823580%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

1-(4-methoxyphenyl)-1H-indole (synthesised from indole by an arylation process analogous to that described in step (a) of Example 1 [arylation process also described in J. Org. Chem. 2008, 73 (14), 5529-5535], 1.0 g, 4.48 mmol), 2-(methylthio)isoindoline-1,3-dione (0.95 g, 4.93 mmol) and magnesium bromide (8 mg, 0.045 mmol) were mixed in degassed DMA and stirred under an atmosphere of nitrogen at 90° C. for 90 min. 1M NaOH and EtOAc were added. The phases were separated and the organic solvents were evaporated. The residue was purified by flash chromatography with heptane/EtAc 20:1 to provide 1-(4-methoxyphenyl)-3-(methylthio)-1H-indole in 80% yield. ES/MS m/z: 270.11 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08653072B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-a15b7cb847614fe0bf15da0edb31229b
Quellennotizuspto-grants-2014_02