HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537258Generated: October 30, 2026
Benzyl mercaptan → 4-(Benzylthio)-2-(trifluoromethyl)pyridine
https://huagongshe.com/reaction/537258
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 4-Chloro-2-(trifluoromethyl)pyridine | HCID 14761442 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(Benzylthio)-2-(trifluoromethyl)pyridine | HCID 86709992 | 75.5% |
Reaction Steps
4-Chloro-2-(trifluoromethyl)pyridine (141 μl, 1.102 mmol), 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) (199 μl, 1.322 mmol), and phenylmethanethiol (129 μl, 1.102 mmol) were dissolved in dry dimethylformamide (2 mL). The reaction mixture was heated at 100° C. in a microwave for 30 minutes, then partitioned between ether (25 mL) and water (25 mL). The aqueous layer was extracted with ether (2×25 mL) and the combined organic layers were 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: 0-30% ethyl acetate in isohexane) to afford 4-(benzylthio)-2-(trifluoromethyl)pyridine (224 mg) as a colourless oil. LCMS (Method F, ES-API): RT 2.79 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-e0ca3873eff24a739d20d876cc7fa909 |
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| Source note | uspto-grants-2014_10 |
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