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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703214Generated: 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/703214

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 numberUS04981865
Source datasetuspto-grants-1991_01
ORD IDord-91a6e64ec51f43fda95a89367f6fc1cf
Source noteuspto-grants-1991_01