HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644828Generated: October 30, 2026
Hydrochloric Acid → HCID 17862344, compound
https://huagongshe.com/reaction/644828
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,5-Difluoronitrobenzene | HCID 67767 | — |
| Reactant | 3H-Pyrazol-3-one, 2,4-dihydro-5-methyl- | HCID 319771 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 17862344 | HCID 17862344 | 48.8% |
Reaction Steps
Potassium carbonate (3.19 g, 23.1 mmol) and 2,5-difluoronitrobenzene (7.34 g, 46.1 mmol) were added to a solution of 3-hydroxy-5-methylpyrazole (4.52 g, 46.1 mmol) in DMF (80 ml) at room temperature, and the mixture was stirred at room temperature overnight. After completion of the reaction, the reaction mixture was poured into 1N hydrochloric acid (100 ml) and extracted with ethyl acetate (100 ml×2). An organic layer was washed with water (100 ml×2), dried over anhydrous magnesium sulfate and filtered to remove magnesium sulfate, 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 3-(4-fluoro-2-nitrophenyloxy)-5-methylpyrazole (5.33 g, yield: 48.8%). mp: 81-84° C.; 1H-NMR (CDCl3, TMS, ppm): δ 2.28 (d, J=0.5 Hz, 3H), 5.71 (d, J=0.5 Hz, 1H), 7.26-7.38 (m, 2H), 7.69 (dd, J=2.8 and 7.9 Hz, 1H), 9.33 (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-8cb7d985fcaa4629abe0d1c10e8b9ce5 |
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| Source note | uspto-grants-2010_04 |
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