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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 332082Erstellt: 24. Oktober 2026

Methyl Ethyl Ketone → 5-Bromo-2,3-dimethyl-1H-indole

https://huagongshe.com/de/reaction/332082

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl Ethyl KetoneHCID 6569—
Edukt4-Bromophenylhydrazine hydrochlorideHCID 12157—
LösungsmittelEthanolHCID 702—
Produkt5-Bromo-2,3-dimethyl-1H-indoleHCID 1279309767%

Reaktionsschritte

Following a published procedure (Gundersen, E. G. U.S. Patent App. Publ. US 2005/070592) 2-Butanone (0.11 mL, 1.278 mmol) was added to a solution of 4-bromophenylhydrazine hydrochloride (0.300 g, 1.342 mmol in EtOH (3.8 mL). The mixture was heated to reflux for 22 h, concentrated in vacuo, and partitioned between EtOAc and 1N HCl. The organic layer was washed with H2O and saturated aqueous NaHCO3, dried over Na2SO4, filtered, and concentrated. The crude residue was purified by chromatography (SiO2, 0-20% EtOAc/Hexane) to afford the desired indole as a pink powder (200 mg, 67%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08877797B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-76b085d4ce4d43bf909b7b7a61b3c790
Quellennotizuspto-grants-2014_11