HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644869Generated: October 30, 2026
Hydrochloric Acid → HCID 17862363, compound
https://huagongshe.com/reaction/644869
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl isocyanate | HCID 8022 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 59263972 | HCID 59263972 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 17862363 | HCID 17862363 | 21% |
Reaction Steps
Triethylamine (0.20 g, 2.0 mmol) and ethyl isocyanate (0.14 g, 2.0 mmol) were added to a solution of 3-(2,6-difluoro-4-trifluoromethylphenyloxy)-5-methylpyrazole (0.42 g, 1.5 mmol) in ethyl acetate (10 ml), and the mixture was stirred at room temperature for 12 hours. After completion of the reaction, the reaction mixture was poured into 2N hydrochloric acid and extracted with ethyl acetate (10 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 (chloroform), to give a white solid of N-ethyl-3-(2,6-difluoro-4-trifluoromethylphenyloxy)-5-methylpyrazole-1-carboxamide (0.11 g, yield: 21.0%). mp: 102-104° C.; 1H-NMR (CDCl3, TMS, ppm): δ 1.21 (t, J=7.3 Hz, 3H), 2.19 (s, 3H), 3.32 (dq, J=6.0 and 7.3 Hz, 2H), 5.00-5.25 (m, 1H), 6.25 (s, 1H), 7.36 (d, JHF=7.0 Hz, 2H).
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-669a765455e14a00a0a3b355038a062b |
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| Source note | uspto-grants-2010_04 |
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