HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386882Generated: November 1, 2026
Acetic Acid → 2-Methyl-4-methylsulfonyl-3-(4-methylsulfonylphenyl)benzoic acid
https://huagongshe.com/reaction/1386882
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | 2-Methyl-4-methylsulfonyl-3-(4-methylthiophenyl)benzoic Acid | HCID 53894549 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Methyl-4-methylsulfonyl-3-(4-methylsulfonylphenyl)benzoic acid | HCID 21183143 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06265606B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-ebf80b1a8530491b8c30396748059ab6 |
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| Source note | uspto-grants-2001_07 |
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