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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886041Generated: November 1, 2026

Methanol → 2-(methylsulfonyl)-1H-benzimidazole

https://huagongshe.com/reaction/1886041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2-(Methylthio)benzimidazoleHCID 23539—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventWaterHCID 962—
Product2-(methylsulfonyl)-1H-benzimidazoleHCID 30352689%

Reaction Steps

According to the procedure of B. M. Trost, et al., Tetrahedron Lett., 22 (14), 1287 (1981), to a cooled (0° C.), stirred solution of 2-(methylthio)benzimidazole (14.5 g, 0.088 mol) in MeOH (350 mL) was added a solution of oxone (2 KHSO5.KHSO4.K2SO4 ; 81.6 g, 0.133 mol) in H2O (350 mL) over 10 minutes. The cooling bath was removed after 10 minutes, stirring was continued at room temperature for 5 hours. The MeOH was removed under reduced pressure and the white solid was collected by filtration to give 15.5 g (89%) of product m.p. 200°-202° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05149700
Source datasetuspto-grants-1992_09
ORD IDord-723a5151c3224c8488cb2c639e08ca45
Source noteuspto-grants-1992_09