HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402910Generated: October 31, 2026
HCID 86684915, compound → HCID 86684914, compound
https://huagongshe.com/reaction/2402910
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 86684915 | HCID 86684915 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 86684914 | HCID 86684914 | 98.8% |
Reaction Steps
4-(4-tert-Butylsulfanyl-3-trifluoromethyl-phenyl)-1-methyl-1H-pyrazole (40.0 g, 127 mmol) was suspended in hydrochloric acid (25% w/w, 780 mL) and stirred at 100° C. under reflux. Part of the hydrochloric acid was distilled off (ca. 80 mL). After the reaction was complete as shown by HPLC, it was cooled to 85° C., water (240 mL) was added, and the mixture was cooled further to 20° C. The pH was adjusted to 4.0 by addition of a solution of sodium hydroxide (32% w/w, ca. 480 mL) in water (960 mL). The aqueous phase was extracted with 2-methyltetrahydrofuran (2×320 mL), the combined organic extracts were washed with a solution of sodium chloride (40.0 g) in water (400 mL) and concentrated in vacuo. The residue was redissolved in tetrahydrofuran (260 mL), concentrated in vacuo, dissolved again in tetrahydrofuran (110 mL) and filtered in order to remove inorganic salts. The precipitate was washed with tetrahydrofuran (30 mL) and the combined filtrate was concentrated in vacuo to obtain the title compound as light brown solid (32.4 g, 98.6%), that was used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08796471B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-6dc47b1adb864ddfb9ebde847d89a4ba |
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| Source note | uspto-grants-2014_08 |
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