Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35479Generated: October 29, 2026

Methanol → 2-[[(4-Methoxy-3,5-dimethyl-2-pyridyl)methyl]sulphinyl]-5-(trifluoromethyl)benzimidazole

https://huagongshe.com/reaction/35479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2-[[(4-Methoxy-3,5-dimethyl-2-pyridyl)methyl]thio]-5-(trifluoromethyl)benzimidazoleHCID 10429026—
SolventDichloromethaneHCID 6344—
Product2-[[(4-Methoxy-3,5-dimethyl-2-pyridyl)methyl]sulphinyl]-5-(trifluoromethyl)benzimidazoleHCID 9886300—

Reaction Steps

31.4 g of 2-[[(4-methoxy-3,5-dimethyl-2-pyridyl)methyl]thio]-5-(trifluoromethyl)benzimidazole are dissolved in 1.3 l of methylene chloride and 50 ml of methanol and then cooled to -20°. 16.9 g of m-chloroperbenzoic acid, recrystallized from a methyene 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 120 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-[[(4-methoxy-3,5-dimethyl-2-pyridyl)methyl]sulphinyl]-5-(trifluoromethyl)benzimidazole of melting point 152°-154°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04766133
Source datasetuspto-grants-1988_08
ORD IDord-7829d988bc3340d3bea8f2c0b997b908
Source noteuspto-grants-1988_08