HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644914Generated: October 30, 2026
Sulfuryl chloride → HCID 17862337, compound
https://huagongshe.com/reaction/644914
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | HCID 17862417 | HCID 17862417 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 17862337 | HCID 17862337 | 84.8% |
Reaction Steps
Sulfuryl chloride (0.16 g, 1.2 mmol) was added to a solution of N-hexyl-3-(2,6-dichloro-4-trifluoromethylphenyloxy)-5-methylpyrazole-1-carboxamide (0.44 g, 1.0 mmol) in acetic acid (5 ml), and the mixture was stirred at room temperature for 4 hours. After completion of the reaction, the reaction mixture was poured into ice water 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. 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-hexyl-4-chloro-3-(2,6-dichloro-4-trifluoromethylphenyloxy)-5-methylpyrazole-1-carboxamide (0.40 g, yield: 84.8%). mp: 86-88° C.; 1H-NMR (CDCl3, TMS, ppm): δ 0.88 (t, J=6.8 Hz, 3H), 1.26 (m, 6H), 1.40-1.60 (m, 2H), 2.62 (s, 3H), 3.15-3.35 (m, 2H), 6.50-6.70 (m, 1H), 7.67 (s, 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-553cdce0db0b450eb5f9793ae4d60caf |
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| Source note | uspto-grants-2010_04 |
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