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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 329139Erstellt: 26. Oktober 2026

2,4,6-Trimethylbenzyl chloride → 2-(2,4,6-trimethylphenylmethylthio)pyridine N-oxide

https://huagongshe.com/reaction/329139

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,4,6-Trimethylbenzyl chlorideHCID 74108—
EduktSodiumHCID 5360545—
EduktHCID 178526253HCID 178526253—
LösungsmittelEthanolHCID 702—
Produkt2-(2,4,6-trimethylphenylmethylthio)pyridine N-oxideHCID 2205478188,7%

Reaktionsschritte

A mixture of 17 gms (0.05 mole) 2-mercaptopyridine N-oxide, sodium salt (40% aqueous solution) and 8.5 gms (0.05 mole) α2 chloroisodurene in 50 ml of ethanol is brought to reflux for 15 minutes. The volatiles are removed and the residue extracted with 150 ml of boiling chloroform, filtered and dried over sodium sulfate. Evaporation and trituration of the residue with a few drops of acetone induce crystallization. A yield of 11.5 gms of 2-(2,4,6-trimethylphenylmethylthio)pyridine N-oxide is obtained. Melting point 137° - 138° C. Structure confirmed by IR and NMR.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04019893
Quelldatensatzuspto-grants-1977_04
ORD IDord-aab389400d344cb691183917617e1f32
Quellennotizuspto-grants-1977_04