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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 342767Erstellt: 25. Oktober 2026

Benzene, 1-chloro-4-fluoro- → 5-allyloxy-N-(4-chlorophenyl)indole

https://huagongshe.com/reaction/342767

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzene, 1-chloro-4-fluoro-HCID 9604—
EduktSodium hydrideHCID 24758—
Edukt5-(prop-2-en-1-yloxy)-1H-indoleHCID 14239230—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-allyloxy-N-(4-chlorophenyl)indoleHCID 54410488—

Reaktionsschritte

To a solution of sodium hydride (60%, 254 mg, 6.35 mmol) in 15 mL tetrahydrofuran (THF) was added 5-allyloxyindole (Step A; 1.0 g, 5.77 mmol) in 5 mL THF and the mixture was stirred for 1 hour at ambient temperature. 4-fluorochlorobenzene (0.69 mL, 6.35 mmol) was added and the reaction heated to reflux for 21 hours. After cooling, the reaction was quenched with saturated aqueous ammonium chloride and extracted with ethyl acetate. The organic layer was washed with water, brine, dried over magnesium sulfate, filtered, concentrated in vacuo, and the crude residue purified by flash chromatography on silica gel (15% ethyl acetate/hexane) to provide the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05859051
Quelldatensatzuspto-grants-1999_01
ORD IDord-795c175dcce247b2aacf26afcf06a6ac
Quellennotizuspto-grants-1999_01