HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644838Generated: October 30, 2026
Hydrochloric Acid → 3-(2-Chloro-6-fluoro-4-trifluoromethylphenyloxy)-5-methylpyrazole
https://huagongshe.com/reaction/644838
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3H-Pyrazol-3-one, 2,4-dihydro-5-methyl- | HCID 319771 | — |
| Reactant | Benzene, 1-chloro-2,3-difluoro-5-(trifluoromethyl)- | HCID 2736496 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(2-Chloro-6-fluoro-4-trifluoromethylphenyloxy)-5-methylpyrazole | HCID 17862428 | 33.8% |
Reaction Steps
Potassium carbonate (1.66 g, 12 mmol) was added to a solution of 3-hydroxy-5-methylpyrazole (2.45 g, 25.0 mmol) and 3-chloro-4,5-difluorobenzotrifluoride (2.5 g, 25.0 mmol) in DMF (40 ml), and the mixture was stirred under heating at 70° 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=1/5), to give a white solid of 3-(2-chloro-6-fluoro-4-trifluoromethylphenyloxy)-5-methylpyrazole (2.29 g, yield: 33.8%). mp: 171-174° C.; 1H-NMR (CDCl3, TMS, ppm): δ 2.27 (s, 3H), 5.71 (s, 1H), 7.37 (dd, JHF=1.8 and 9.4 Hz, 1H), 7.54 (s, 1H), 8.85-9.55 (br s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700786B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-bbe9b8563ab547a88383120e0eba40e2 |
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| Source note | uspto-grants-2010_04 |
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