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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217141Generated: October 25, 2026

Pyrazole → 1-(5-Bromo-3-fluoro-2-nitro-phenyl)-1H-pyrazole

https://huagongshe.com/reaction/217141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrazoleHCID 1048—
ReactantSodium hydrideHCID 24758—
Reactant5-Bromo-1,3-difluoro-2-nitrobenzeneHCID 21335487—
SolventTetrahydrofuranHCID 8028—
Product1-(5-Bromo-3-fluoro-2-nitro-phenyl)-1H-pyrazoleHCID 6700464886%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of sodium hydride (44 mg, 1.1 mmol, 60% oil dispersion) in THF (4 mL), stirred at 0° C., was added a solution of pyrazole (72 mg, 1.05 mmol) in THF (1 mL). The resulting mixture was stirred at 0° C. for 5 minutes and a solution of 5-bromo-1,3-difluoro-2-nitro-benzene (238 mg, 1 mmol) in THF (1 mL) was added. The mixture was stirred at room temperature for 1 hour, quenched by addition of water (1 mL), then partitioned between water (20 mL) and ethyl acetate (50 mL). The organic layer was washed with brine, dried (MgSO4), and concentrated in vacuo. The residue was purified by column chromatography over silica gel eluted with ethyl acetate:hexanes (1:6), to afford 240 mg (86%) of the title compound. 1H NMR (CDCl3) δ 6.55 (t, 1H), 7.45 (d, 1H), 7.60 (s, 1H), 7.80 (m, 2H). MS M+1 287, M+1+2 289.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193352B2
Source datasetuspto-grants-2012_06
ORD IDord-18cf073f84af497e87c3739ab11ab8f0
Source noteuspto-grants-2012_06