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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848981Generated: October 31, 2026

Acetic Acid → 2-Methyl-4-methylsulfonyl-3-(4-methylsulfonylphenyl)benzoic acid

https://huagongshe.com/reaction/848981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrogen PeroxideHCID 784—
ReactantSodium BisulfiteHCID 23665763—
Reactant2-Methyl-4-methylsulfonyl-3-(4-methylthiophenyl)benzoic AcidHCID 53894549—
SolventWaterHCID 962—
Product2-Methyl-4-methylsulfonyl-3-(4-methylsulfonylphenyl)benzoic acidHCID 21183143—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2.2 g (6.5 mmol) of 2-methyl-4-methylsulfonyl-3-(4-methylthiophenyl)benzoic acid, 2.2 mL (19.6 mmol) of 30 percent hydrogen peroxide, and 25 mL of acetic acid was heated to 80° C. with stirring for 1 hour and was then allowed to stand overnight. The mixture was diluted with water, treated with sodium bisulfite, and then extracted with a mixture of ether and ethyl acetate. The extract was concentrated by evaporation under reduced pressure and the residue was diluted with dichloromethane. The resulting mixture was filtered and the solids that were collected were washed with ethyl acetate. The filtrate was found to contain only about 0.5 g of impure product and was discarded. The solids were dissolved (a slow process) in a mixture of ethyl acetate and water and the organic phase was separated and concentrated by evaporation under reduced pressure. The resulting solid residue was diluted with hexane and the insoluble solids were recovered by filtration and dried to obtain 2.1 g (88 percent of theory) of the title compound as a white powder melting at 214-215° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06010981
Source datasetuspto-grants-2000_01
ORD IDord-7d32b4ebba504f7585eda722e33fd2dd
Source noteuspto-grants-2000_01