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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387068Generated: November 1, 2026

Pyrazole → 1-(4-Bromo-2-ethyl-benzyl)-1H-pyrazole

https://huagongshe.com/reaction/2387068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrazoleHCID 1048—
Reactant4-Bromo-1-(bromomethyl)-2-ethylbenzeneHCID 58764075—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-(4-Bromo-2-ethyl-benzyl)-1H-pyrazoleHCID 5876416680%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of pyrazole (616 mg, 9.1 mmol) in anhydrous DMF (30 mL) was treated with naH (60%, 362 mg). 4-Bromo-1-bromomethyl-2-ethyl-benzene (2.5 g, 9.1 mmol) was added and the resulting solution was stirred at 80° C. for 13 hours before it was cooled down to room temperature. The mixture was diluted with H2O, extracted with Et2O. The combined organic extracts were washed with H2O, brine, dried over MgSO4 and concentrated under reduced pressure. The residue was purified by flash column chromatography to afford the desired product (1.92 g, 80% yield). 1H NMR (300 MHz, CDCl3): δ 1.15 (t, J=7.5 Hz, 3 H), 2.59-2.66 (m, 2 H), 5.30 (s, 2 H), 6.26-6.28 (m, 1 H), 6.86-6.88 (m, 1 H), 7.29-7.32 (m, 2 H), 7.37-7.38 (m, 1 H), 7.54-7.55 (m, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268835B2
Source datasetuspto-grants-2012_09
ORD IDord-2b9a01d1c52b42af8b2c5384ab7da086
Source noteuspto-grants-2012_09