HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644842Generated: October 30, 2026
Hydrochloric Acid → 3-(3-Chloro-5-trifluoromethylpyridin-2-yloxy)-5-methylpyrazole
https://huagongshe.com/reaction/644842
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,3-Dichloro-5-(trifluoromethyl)pyridine | HCID 112234 | — |
| Reactant | 3H-Pyrazol-3-one, 2,4-dihydro-5-methyl- | HCID 319771 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(3-Chloro-5-trifluoromethylpyridin-2-yloxy)-5-methylpyrazole | HCID 17862457 | 76% |
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 2,3-dichloro-5-trifluoromethylpyridine (10.8 g, 50.0 mmol) in DMF (50 ml) at room temperature, 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 (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=1/2), to give a white solid of 3-(3-chloro-5-trifluoromethylpyridin-2-yloxy)-5-methylpyrazole (10.5 g, yield: 76.0%). mp: 93-95° C.; 1H-NMR (CDCl3, TMS, ppm): δ 2.32 (s, 3H), 5.90 (s, 1H), 7.98 (d, J=2.0 Hz, 1H), 8.33 (m, 1H), 10.80-11.60 (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-e41bc377a4604567a4756ce158f3ef90 |
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| Source note | uspto-grants-2010_04 |
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