HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644896Generated: October 30, 2026
Hydrochloric Acid → N-methoxymethyl-3-(2,6-dichloro-4-trifluoromethylphenyloxy)-5-methylpyrazole-1-carbothioamide
https://huagongshe.com/reaction/644896
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methoxymethyl isothiocyanate | HCID 140624 | — |
| Reactant | 3-(2,6-Dichloro-4-trifluoromethylphenyloxy)-5-methylpyrazole | HCID 17862360 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-methoxymethyl-3-(2,6-dichloro-4-trifluoromethylphenyloxy)-5-methylpyrazole-1-carbothioamide | HCID 17862362 | 46.7% |
Reaction Steps
Potassium carbonate (0.23 g, 1.7 mmol) and methoxymethyl isothiocyanate (0.16 g, 1.5 mmol) were added to a solution of 3-(2,6-dichloro-4-trifluoromethylphenyloxy)-5-methylpyrazole (0.47 g, 1.5 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 white solid of N-methoxymethyl-3-(2,6-dichloro-4-trifluoromethylphenyloxy)-5-methylpyrazole-1-carbothioamide (0.29 g, yield: 46.7%). mp: 95-96° C.; 1H-NMR (CDCl3, TMS, ppm): δ 2.82 (d, J=0.6 Hz, 3H), 3.41 (s, 3H), 5.10 (d, J=6.3 Hz, 2H), 5.91 (q, J=0.6 Hz, 1H), 7.68 (s, 2H), 8.80-9.20 (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-abe482d8c6e3469cbe6ba9bb81d024a4 |
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| Source note | uspto-grants-2010_04 |
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