HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644871Generated: October 30, 2026
Hydrochloric Acid → HCID 17862437, compound
https://huagongshe.com/reaction/644871
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl isocyanate | HCID 8022 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 17862427 | HCID 17862427 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 17862437 | HCID 17862437 | 16.6% |
Reaction Steps
Potassium carbonate (0.30 g, 2.2 mmol) and ethyl isocyanate (0.14 g, 2.0 mmol) were added to a solution of 3-(2-chloro-6-nitro-4-trifluoromethylphenyloxy)-5-methylpyrazole (0.64 g, 2.0 mmol) in ethyl acetate (10 ml), and the mixture was stirred at room temperature overnight. 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 (ethyl acetate/hexane=1/10), to give a yellowish solid of N-ethyl-3-(2-chloro-6-nitro-4-trifluoromethylphenyloxy)-5-methylpyrazole-1-carboxamide (0.13 g, yield: 16.6%). mp: 98-99° C.; 1H-NMR (CDCl3, TMS, ppm): δ 1.18 (t, J=7.2 Hz, 3H), 2.60 (d, J=0.5 Hz, 3H), 3.32 (dq, J=6.0 and 7.2 Hz, 2H), 5.87 (q, J=0.5 Hz, 1H), 6.40-6.65 (m, 1H), 8.01 (d, J=2.0 Hz, 1H), 8.17 (m, 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-a69a236f71b842758dc8cfddc03cf16f |
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| Source note | uspto-grants-2010_04 |
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