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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402910Generated: October 31, 2026

HCID 86684915, compound → HCID 86684914, compound

https://huagongshe.com/reaction/2402910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86684915HCID 86684915—
SolventHydrochloric AcidHCID 313—
ProductHCID 86684914HCID 8668491498.8%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796471B2
Source datasetuspto-grants-2014_08
ORD IDord-6dc47b1adb864ddfb9ebde847d89a4ba
Source noteuspto-grants-2014_08