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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1196864Erstellt: 26. Oktober 2026

Pyridine → 4-[(Chloromethyl)sulfanyl]pyridine

https://huagongshe.com/reaction/1196864

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktChlorosuccinimideHCID 31398—
Edukt4-(Methylthio)pyridineHCID 140938—
LösungsmittelBenzeneHCID 241—
Produkt4-[(Chloromethyl)sulfanyl]pyridineHCID 1370398146,5%

Reaktionsschritte

A solution of 4-methylthiopyridine (2.28 g, 18.2 mmol), N-chlorosuccinimide (3.0 g, 23 mmol) and pyridine (2.9 mL, 3.0 mmol) in benzene (40 mL) was heated at 50°-60° C. for 3 h. The mixture was allowed to cool to room temperature. The solvent was decanted and the residue was rinsed with benzene (2×10 mL). The organic phases were combined and evaporated. The residue was passed through a pad of silica gel (40 g) to give the title material (1.35 g) contaminated with the starting material. The impure product was repurified on silica gel preparative plates (eluted with CH2Cl2 /CH3CN: 1/1) to give the pure title material (926 mg, 32%) as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05116833
Quelldatensatzuspto-grants-1992_05
ORD IDord-abb8f79711af4e5884a112e7965ac866
Quellennotizuspto-grants-1992_05