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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540546Generated: October 26, 2026

Selectfluor → 4-Fluoro-5-(2-methoxy-5-nitro-phenyl)-1-methyl-1H-pyrazole

https://huagongshe.com/reaction/540546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSelectfluorHCID 2724933—
Reactant5-(2-Methoxy-5-nitrophenyl)-1-methyl-1H-pyrazoleHCID 23139531—
SolventAcetonitrileHCID 6342—
SolventHCID 178435178HCID 178435178—
Product4-Fluoro-5-(2-methoxy-5-nitro-phenyl)-1-methyl-1H-pyrazoleHCID 2313943033.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

5-(2-Methoxy-5-nitro-phenyl)-1-methyl-1H-pyrazole (300.0 mg, 1.29 mmol) was dissolved in ACN (15 ml) in a polypropylene 20 mL scintillation vial. To this solution, Selectfluor (913.9 mg, 2.58 mmol) was added and the mixture was degassed with argon and heated to 80° C. for 6 hours. The solvent was removed under reduced pressure and the residue was dissolved in 50 mL EtOAc and 30 mL 3N HCl. The organic layer was separated and the aqueous layer was extracted with EtOAc (2×50 ml). The organic layers were combined, dried over Na2SO4, filtered, and the solvent removed under reduced pressure. The residue was then purified by flash chromatography (Biotage SiO2, Hexanes (0.01% TEA)/EtOAc gradient elution) to afford 108 mg (33%) of 4-fluoro-5-(2-methoxy-5-nitro-phenyl)-1-methyl-1H-pyrazole as a white solid. LCMS m/z (%)=252 (M+H, 100). 1H NMR (400 MHz, CDCl3) δ: 8.39 (d, J=9.2 Hz, 1H), 8.22 (s, 1H), 7.44 (d, JH,F=4.4 Hz, 1H), 7.12 (d, J=9.2 Hz, 1H) 3.98 (s, 3H), 3.77 (s, 3H). 19F NMR (376 MHz, CDCl3) δ: −175.50 (d, JH,F=5.3 Hz, 1F).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871797B2
Source datasetuspto-grants-2014_10
ORD IDord-010edfb0e80c44998c7e00215cbdb916
Source noteuspto-grants-2014_10