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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl mercaptanHCID 7509—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant4-Chloro-2-(trifluoromethyl)pyridineHCID 14761442—
SolventDimethylformamideHCID 6228—
Product4-(Benzylthio)-2-(trifluoromethyl)pyridineHCID 8670999275.5%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859774B2
Source datasetuspto-grants-2014_10
ORD IDord-e0ca3873eff24a739d20d876cc7fa909
Source noteuspto-grants-2014_10