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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1007484Erstellt: 24. Oktober 2026

Ethyl Acetate → 3-Isopropyl-5-(4-nitro-2,6-dimethyl-phenoxy)-1H-indole

https://huagongshe.com/de/reaction/1007484

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktPotassium CarbonateHCID 11430—
Edukt2-Fluoro-1,3-dimethyl-5-nitrobenzeneHCID 11367232—
Edukt3-isopropyl-1H-indol-5-olHCID 22669491—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelWaterHCID 962—
Produkt3-Isopropyl-5-(4-nitro-2,6-dimethyl-phenoxy)-1H-indoleHCID 22669511—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

11.44 g (58.76 mmol) of 5-hydroxy-3-isopropyl-indole are dissolved in 350 ml of DMSO, 8.93 g (64.63 mmol) of potassium carbonate in solid form are introduced and subsequently 9.94 g (58.76 mmol) of 3,5-dimethyl-4-fluoronitrobenzene are added. The reaction solution is stirred for 2 hours at 100° C. under argon. Afterwards it is cooled to room temperature, 100 ml of ethyl acetate and 600 ml of H2O are added; ethyl acetate is separated off after phase separation and the aqueous phase is reextracted twice with ethyl acetate. The combined organic phases are washed twice with sodium chloride solution, dried over sodium sulphate, filtered and concentrated to dryness. The residue is purified by chromatography on silica gel by means of cyclohexane/ethyl acetate (10:1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06794406B2
Quelldatensatzuspto-grants-2004_09
ORD IDord-c65647b50728423e988ab1d275144b03
Quellennotizuspto-grants-2004_09