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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329139Generated: October 26, 2026

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

https://huagongshe.com/reaction/329139

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-Trimethylbenzyl chlorideHCID 74108—
ReactantSodiumHCID 5360545—
ReactantHCID 178526253HCID 178526253—
SolventEthanolHCID 702—
Product2-(2,4,6-trimethylphenylmethylthio)pyridine N-oxideHCID 2205478188.7%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04019893
Source datasetuspto-grants-1977_04
ORD IDord-aab389400d344cb691183917617e1f32
Source noteuspto-grants-1977_04