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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45241Generated: October 25, 2026

Thiophenol → 2-Chloro-5-(phenylthio)pyridine

https://huagongshe.com/reaction/45241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
Reactant2-Chloro-5-iodopyridineHCID 4397176—
ReactantSodium MethoxideHCID 10942334—
CatalystCopperHCID 23978—
SolventMethanolHCID 887—
SolventSodium HydroxideHCID 14798—
Product2-Chloro-5-(phenylthio)pyridineHCID 1119539760%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 3.4 g (14.3 mmol) of 2-chloro-5 iodopyridine, 1.9 g (17.2 mmol) of thiophenol, 0.93 g (17.2 mmol) of sodium methoxide and 0.36 g (5.7 mmol) of copper in 18 mL of MeOH is heated for 12 hours at 80° C. After cooling to room temperature, the medium is taken up in 100 mL of 1N NaOH and the MeOH is evaporated off under reduced pressure. The reaction medium is extracted with EtOAc (2×100 mL), the organic phase is washed with 0.1N NaOH (2×30 mL), and then dried over Na2SO4, concentrated under reduced pressure and purified by chromatography on a column of silica gel, eluting with a cyclohexane/EtOAc mixture (8/2). 1.90 g of 2-chloro-5-(phenylsulfanyl)pyridine are obtained in the form of a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541455B2
Source datasetuspto-grants-2013_09
ORD IDord-54549360e77f43089666cb6f25cc9bf9
Source noteuspto-grants-2013_09