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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195879Generated: October 31, 2026

Benzoic acid, 2-((2,6-dichloro-3-methylphenyl)amino)-, methyl ester → 1-[2-[(2,6-Dichloro-3-methylphenyl)amino]phenyl]-2-(methylsulfinyl)ethanone

https://huagongshe.com/reaction/1195879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic acid, 2-((2,6-dichloro-3-methylphenyl)amino)-, methyl esterHCID 76743—
Reactantdimethylsulfoxide THFHCID 21830753—
SolventTetrahydrofuranHCID 8028—
Product1-[2-[(2,6-Dichloro-3-methylphenyl)amino]phenyl]-2-(methylsulfinyl)ethanoneHCID 1502738226%

Reaction Steps

2-[(2,6-Dichloro-3-methylphenyl)amino]benzoic acid methyl ester (3.3 g, 10.6 mmol) is dissolved in 30 ml of dry THF and added to a solution of dimsyl anion (JACS, 84, 866, 1982) (31.9 mmol) in 60 ml of 1:1 DMSO/THF at 0° C. under argon. When addition is complete, the ice bath is removed and the reaction mixture is stirred at room temperature for five hours. The reaction is quenched with 400 ml of 1N hydrochloric acid, and extracted twice with 300 ml of chloroform. The combined chloroform extract is washed with 300 ml of water three times, and once with 300 ml of brine. This chloroform layer is dried over magnesium sulfate and evaporated. The residue solidifies after being dried at room temperature under vacuum for 12 hours. Recrystallization from methylene chloride in hexane gives 1.0 g of 1-[2-[(2,6-dichloro-3-methylphenyl)amino]phenyl]-2-(methylsulfinyl)ethanone (26% yield); mp 152°-154° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112846
Source datasetuspto-grants-1992_05
ORD IDord-fef424ed9c0b4d1e91a3c2746c49e90f
Source noteuspto-grants-1992_05