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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537260Generated: October 29, 2026

Water → 2-(Benzylthio)-4-(trifluoromethyl)pyridine

https://huagongshe.com/reaction/537260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl mercaptanHCID 7509—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoro-4-(trifluoromethyl)pyridineHCID 11159514—
SolventDimethylformamideHCID 6228—
Product2-(Benzylthio)-4-(trifluoromethyl)pyridineHCID 7221845062.5%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859774B2
Source datasetuspto-grants-2014_10
ORD IDord-7ff81bb7fb634a4da71dc89d9b744e72
Source noteuspto-grants-2014_10