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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663184Generated: October 30, 2026

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

https://huagongshe.com/reaction/1663184

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 numberUS08034832B2
Source datasetuspto-grants-2011_10
ORD IDord-52be805335d446fbad50e02f97de7608
Source noteuspto-grants-2011_10