HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537260Generated: October 29, 2026
Water → 2-(Benzylthio)-4-(trifluoromethyl)pyridine
https://huagongshe.com/reaction/537260
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Fluoro-4-(trifluoromethyl)pyridine | HCID 11159514 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(Benzylthio)-4-(trifluoromethyl)pyridine | HCID 72218450 | 62.5% |
Reaction Steps
To a solution of phenylmethanethiol (356 μl, 3.03 mmol) and 2-fluoro-4-(trifluoromethyl)pyridine (369 μl, 3.03 mmol) in dimethylformamide (5 mL) was added potassium carbonate (628 mg, 4.54 mmol). The reaction mixture was stirred at 60° C. for 2 hours, then cooled to room temperature, water (10 mL) was added, and the mixture was extracted with ethyl acetate (3×15 mL). The combined organic layers were washed with saturated aqueous sodium hydrogen carbonate solution (20 mL), brine (20 mL), dried over magnesium sulfate, filtered and concentrated in vacuo to give a pale yellow oil. The crude product was purified by chromatography on silica gel (gradient: 0-20% ethyl acetate in isohexane) to afford 2-(benzylthio)-4-(trifluoromethyl)pyridine (510 mg) as a colourless oil. LCMS (Method F, ES-API): RT 3.04 min, m+H=270.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859774B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-7ff81bb7fb634a4da71dc89d9b744e72 |
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| Source note | uspto-grants-2014_10 |
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