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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1292965Erstellt: 23. Oktober 2026

Benzyl Bromide → 1-Benzyl-5-nitro-1H-indazole

https://huagongshe.com/de/reaction/1292965

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktPotassium CarbonateHCID 11430—
Edukt5-NitroindazoleHCID 21501—
LösungsmittelAcetonitrileHCID 6342—
Produkt1-Benzyl-5-nitro-1H-indazoleHCID 2195208245,1%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

To a solution of 5-nitroindazole (10.0 g, 61.3 mmol) in acetonitrile (100 mL) was added potassium carbonate (16.9 g, 122.6 mmol) and benzyl bromide (13.6 g, 79.7 mmol). The resulting yellow reaction mixture was heated with stirring at 70° C. overnight. Upon cooling down, the solid was filtered off and washed with methylene chloride. The filtrate was concentrated to dryness and the resulting residue was purified by flash chromatography eluting with 17–25% ethyl acetate in hexanes (v/v) yielding 7.0 g (44%) of the corresponding 1-Benzyl-5-nitro-1H-indazole as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07238701B2
Quelldatensatzuspto-grants-2007_07
ORD IDord-1a4d388626f84811aaef5791b5b36270
Quellennotizuspto-grants-2007_07