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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644832Generated: October 30, 2026

Hydrochloric Acid → HCID 17862346, compound

https://huagongshe.com/reaction/644832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoro-5-nitrobenzotrifluorideHCID 94954—
Reactant3H-Pyrazol-3-one, 2,4-dihydro-5-methyl-HCID 319771—
SolventDimethylformamideHCID 6228—
ProductHCID 17862346HCID 1786234660.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

Potassium carbonate (7.60 g, 55.0 mmol) was added to a solution of 3-hydroxy-5-methylpyrazole (4.90 g, 50.0 mmol) and 2-fluoro-5-nitrobenzotrifluoride (10.5 g, 50.0 mmol) in DMF (50 ml), and the mixture was stirred under heating at 60° C. for 4 hours. After completion of the reaction, the reaction mixture was poured into 2N hydrochloric acid (100 ml) and extracted with ethyl acetate (50 ml×3). An organic layer was washed with water, dried over anhydrous magnesium sulfate and filtered to remove a desiccant, and the solvent was distilled off from the filtrate under reduced pressure. The resultant crude product was purified with a silica gel column (ethyl acetate/hexane=1/3), to give a yellowish viscous substance of 5-methyl-3-(4-nitro-2-trifluoromethylphenyloxy)pyrazole (8.70 g, yield: 60.6%). 1H-NMR (CDCl3, TMS, ppm): δ 2.30 (d, J=0.5 Hz, 3H), 5.78 (d, J=0.5 Hz, 1H), 7.31 (d, J=9.2 Hz, 1H), 8.31 (dd, J=2.7 and 9.2 Hz, 1H), 8.57 (d, J=2.7 Hz, 1H), 10.05-10.50 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700786B2
Source datasetuspto-grants-2010_04
ORD IDord-83a54b2d5a174b11aa8f4036080fc12c
Source noteuspto-grants-2010_04