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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508881Generated: November 2, 2026

Pyrazole → 1-(4-Nitrobenzyl)-1H-pyrazole

https://huagongshe.com/reaction/1508881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrazoleHCID 1048—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Nitrobenzyl bromideHCID 66011—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product1-(4-Nitrobenzyl)-1H-pyrazoleHCID 97366381%

Reaction Steps

A mixture of 4-nitrobenzyl bromide (0.500 g, 2.31 mmol), 1H-pyrazole (0.362 g, 5.23 mmol), and potassium carbonate (0.704 g, 5.09 mmol) in acetonitrile (30 mL) was stirred at rt overnight. After this time, the mixture was diluted with water and extracted with ethyl acetate. The combined organic layer was dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated. The residue was purified by column chromatography (silica, hexanes/ethyl acetate) to afford the title compound (0.380 g, 76%) as a white solid. MW=203.20. 1H NMR (CDCl3, 500 MHz) δ 8.21-8.19 (m, 1H), 8.19-8.16 (m, 1H), 7.61-7.57 (m, 1H), 7.48-7.44 (m, 1H), 7.32-7.28 (m, 2H), 6.35 (t, J=2.1 Hz, 1H), 5.44 (s, 2H); APCI MS m/z 204 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221843B2
Source datasetuspto-grants-2015_12
ORD IDord-4f3eb4d6f2754893a5fe6e8c1a885ee1
Source noteuspto-grants-2015_12