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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35481Generated: October 28, 2026

Methanol → 2-[[(3-Methyl-2-pyridyl)methyl]sulphinyl]-5-(trifluoromethyl)benzimidazole

https://huagongshe.com/reaction/35481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2-[[(3-Methyl-2-pyridyl)methyl]thio]-5-(trifluoromethyl)benzimidazoleHCID 21295864—
SolventDichloromethaneHCID 6344—
Product2-[[(3-Methyl-2-pyridyl)methyl]sulphinyl]-5-(trifluoromethyl)benzimidazoleHCID 21295919—

Reaction Steps

6.7 g of 2-[[(3-methyl-2 -pyridyl)methyl]thio]-5-(trifluoromethyl)benzimidazole are dissolved in 250 ml of methylene chloride and 20 ml of methanol and then cooled to -20°. 4.7 g of m-chloroperbenzoic acid, recrystallized from methylene chloride/petroleum ether, are then introduced within 10 minutes. The solution is stirred further at -20° for 60 minutes and then poured into a mixture of 100 ml of 2N sodium carbonate solution and ice. The organic phase is washed neutral with water, dried over sodium sulphate and evaporated in vacuo. Crystallization from methylene chloride/methanol/petroleum ether gives 2-[[(3-methyl-2-pyridyl)methyl]sulphinyl]-5 -(trifluoromethyl)benzimidazole of melting point 156°-158°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04766133
Source datasetuspto-grants-1988_08
ORD IDord-36f539df287c4cb6b695965756d6b25c
Source noteuspto-grants-1988_08