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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070853Generated: October 26, 2026

Disodium disulfite → 6-[[1-(4-methylphenyl)-2-(phenylmethanesulfinyl)-1H-benzimidazol-6-yl]oxy]hexanoic acid methyl ester

https://huagongshe.com/reaction/1070853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDisodium disulfiteHCID 24346—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant6-[[2-Benzylmercapto-1-(4-methylphenyl)-1H-benzimidazol-6-yl]oxy]Hexanoic Acid Methyl EsterHCID 10162512—
SolventDichloromethaneHCID 6344—
Product6-[[1-(4-methylphenyl)-2-(phenylmethanesulfinyl)-1H-benzimidazol-6-yl]oxy]hexanoic acid methyl esterHCID 1030008144.9%

Reaction Conditions

Temperature20 °C

Reaction Steps

500 mg of 6-[[2-benzylmercapto-1-(4-methylphenyl)-1H-benzimidazol-6-yl]oxy]hexanoic acid methyl ester was dissolved in 9 ml of dichloromethane, mixed with 303 mg of m-chloroperbenzoic acid (about 60%), and the mixture was stirred for 2 hours at 20° C. It was mixed with sodium disulfite solution, extracted twice with dichloromethane, the combined organic phases were washed with saturated sodium bicarbonate solution, water and saturated sodium chloride solution, dried on sodium sulfate and concentrated by evaporation in a vacuum. The residue was purified by column chromatography on silica gel. 232 mg of 6-[[1-(4-methylphenyl)-2-(phenylmethanesulfinyl)-1H-benzimidazol-6-yl]oxy]hexanoic acid methyl ester was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903126B2
Source datasetuspto-grants-2005_06
ORD IDord-29289839d20b49b0a09bb8a6540dfe15
Source noteuspto-grants-2005_06