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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644840Generated: October 29, 2026

Hydrochloric Acid → HCID 17862427, compound

https://huagongshe.com/reaction/644840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant3H-Pyrazol-3-one, 2,4-dihydro-5-methyl-HCID 319771—
Reactant3-Chloro-4-fluoro-5-nitrobenzotrifluorideHCID 2736565—
SolventDimethylformamideHCID 6228—
ProductHCID 17862427HCID 1786242756.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

Sodium hydride (60% in oil, 0.44 g, 11.0 mmol) was added to a solution of 3-hydroxy-5-methylpyrazole (0.98 g, 10.0 mmol) and 3-chloro-4-fluoro-5-nitrobenzotrifluoride (1.5 g, 10.0 mmol) in DMF (30 ml), and the mixture was stirred under heating at 60° C. for 7 hours. After completion of the reaction, the reaction mixture was poured into 2N hydrochloric acid (80 ml) and extracted with ethyl acetate (30 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=1/7→1/3), to give a yellowish solid of 3-(2-chloro-6-nitro-4-trifluoromethylphenyloxy)-5-methylpyrazole (1.8 g, yield: 56.6%). mp: 120-123° C.; 1H-NMR (CDCl3, TMS, ppm): δ 2.29 (s, 3H), 5.79 (s, 1H), 7.98 (d, J=1.8 Hz, 1H), 8.17 (d, J=1.8 Hz, 1H), 8.65-9.30 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700786B2
Source datasetuspto-grants-2010_04
ORD IDord-ac7c763208bc4738b8b5ac81315a4997
Source noteuspto-grants-2010_04