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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 351576Erstellt: 24. Oktober 2026

Water → 7-Ethenyl-1H-indole

https://huagongshe.com/de/reaction/351576

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktTributylvinyltinHCID 81998—
EduktLithium ChlorideHCID 433294—
Edukt7-BromoindoleHCID 2757020—
KatalysatorTriphenylphosphineHCID 11776—
KatalysatorHCID 178479785HCID 178479785—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt7-Ethenyl-1H-indoleHCID 1456740480%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To 7-bromo-1H-indole (6.0 g, 30.6 mmol) in 150 mL of dimethylformamide was added tributyl(vinyl)tin (9.8 mL, 33.7 mmol), triphenylphosphine (0.4 g, 1.53 mmol), diphenyl-palladium(II) dichloride (1.07 g, 1.53 mmol) and lithium chloride (4.0 g, 94.4 mmol), and the resulting mixture was heated at 100° C. overnight. The reaction mixture was cooled to 20-24° C. and poured into 150 mL of water and 150 mL of ethyl acetate. The aqueous layer was washed with additional ethyl acetate (3×100 mL) and the combined organic layers were washed with saturated aqueous sodium chloride, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The residue was subjected to silica gel chromatography, eluting with 5-10% ethyl acetate in hexanes. Fractions containing product were combined and concentrated under reduced pressure to provide 3.5 g (80%) of the desired compound as a clear oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06743785B2
Quelldatensatzuspto-grants-2004_06
ORD IDord-0cfbd83475514974a0e7c40b96b6fc3f
Quellennotizuspto-grants-2004_06