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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537255Generated: October 29, 2026

Methanol → 2-(Benzylthio)-6-(trifluoromethyl)pyridine

https://huagongshe.com/reaction/537255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBenzyl mercaptanHCID 7509—
ReactantSodium hydrideHCID 24758—
Reactant2-Fluoro-6-(trifluoromethyl)pyridineHCID 2736501—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product2-(Benzylthio)-6-(trifluoromethyl)pyridineHCID 7221308169.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of sodium hydride (0.170 g, 4.24 mmol) in tetrahydrofuran (10 mL) was added phenylmethanethiol (0.338 ml, 2.88 mmol) dropwise at 0° C. The reaction mixture was stirred at 0° C. for 15 minutes then 2-fluoro-6-(trifluoromethyl)pyridine (0.365 ml, 3.03 mmol) was added dropwise. The reaction mixture was stirred at 0° C. for 30 minutes. Methanol (1 mL) was added carefully and the reaction mixture was stirred at 0° C. for a further 10 minutes then water (5 mL) and dichloromethane (10 mL) were added. The organic layer was recovered using a phase separator cartridge then concentrated in vacuo to give 2-(benzylthio)-6-(trifluoromethyl)pyridine (538 mg) as a colourless oil. LCMS (Method F, ES-API): RT 2.80 min, m+H=270.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859774B2
Source datasetuspto-grants-2014_10
ORD IDord-1a762b3af496432996c4594a971641df
Source noteuspto-grants-2014_10