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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1200010Generated: November 3, 2026

4-Methoxy-alpha-toluenethiol → 4-Cyano-3-(4-methoxyphenyl)methylmercaptopyridine

https://huagongshe.com/reaction/1200010

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxy-alpha-toluenethiolHCID 80407—
Reactant3-Chloropyridine-4-carbonitrileHCID 10678306—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
SolventSodium MethoxideHCID 10942334—
Product4-Cyano-3-(4-methoxyphenyl)methylmercaptopyridineHCID 1427764860%

Reaction Steps

A solution of 6.2 g (40 mmol) of p-methoxybenzylmercaptan in 9.8 mL of 4.4M sodium methoxide in methanol was added dropwise to a solution of 5.52 g (40 mmol) of 3-chloro-4-cyanopyridine in dry acetonitrile that has been cooled in an ice bath. After addition was complete the solution was allowed to warm to room temperature over 2 hours. The solvent was concentrated and the residue was partitioned between dichloromethane and water. The aqueous layer was extracted with two portions of dichloromethane and the combined extracts were washed with brine, dried (MgSO4) and concentrated to afford 6.1 g (60%) of a pale yellow crystalline solid, m.p. 80°-81° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04904672
Source datasetuspto-grants-1990_02
ORD IDord-347ca1233e97461c9fdc3a9bc09ef488
Source noteuspto-grants-1990_02