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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292965Generated: October 26, 2026

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

https://huagongshe.com/reaction/1292965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant5-NitroindazoleHCID 21501—
SolventAcetonitrileHCID 6342—
Product1-Benzyl-5-nitro-1H-indazoleHCID 2195208245.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238701B2
Source datasetuspto-grants-2007_07
ORD IDord-1a4d388626f84811aaef5791b5b36270
Source noteuspto-grants-2007_07