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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644831Generated: October 31, 2026

Hydrochloric Acid → HCID 17862373, compound

https://huagongshe.com/reaction/644831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Fluoro-3-nitrobenzotrifluorideHCID 67778—
Reactant3H-Pyrazol-3-one, 2,4-dihydro-5-methyl-HCID 319771—
SolventDimethylformamideHCID 6228—
ProductHCID 17862373HCID 1786237370.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

Potassium carbonate (9.12 g, 66.0 mmol) was added to a solution of 3-hydroxy-5-methylpyrazole (5.88 g, 60.0 mmol) and 4-fluoro-3-nitrobenzotrifluoride (12.6 g, 60.0 mmol) in DMF (120 ml), and the mixture was stirred at 50° C. for 4 hours. After completion of the reaction, the reaction mixture was poured into 2N hydrochloric acid (200 ml) and extracted with ethyl acetate (70 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 yellow solid of 5-methyl-3-(2-nitro-4-trifluoromethylphenyloxy)pyrazole (12.1 g, yield: 69.0%). mp: 89-91° C.; 1H-NMR (CDCl3, TMS, ppm): δ 2.28 (s, 3H), 5.77 (s, 1H), 7.40 (d, J=8.8 Hz, 1H), 7.76 (dd, J=2.0 and 8.8 Hz, 1H), 8.21 (d, J=2.0 Hz, 1H), 10.10-11.05 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700786B2
Source datasetuspto-grants-2010_04
ORD IDord-7c01960f2b6e426e8223443687ce823b
Source noteuspto-grants-2010_04