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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 563955Generated: October 26, 2026

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

https://huagongshe.com/reaction/563955

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 numberUS08067606B2
Source datasetuspto-grants-2011_11
ORD IDord-31616cd2eabe4d528f50aabcf300ecb5
Source noteuspto-grants-2011_11