HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380068Generated: October 31, 2026
Acetic Acid → p-(Methylsulphonyl)benzoic acid
https://huagongshe.com/reaction/2380068
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | 4-(Methylthio)benzoic acid | HCID 83230 | — |
| Solvent | Water | HCID 962 | — |
| Product | p-(Methylsulphonyl)benzoic acid | HCID 77670 | 88.1% |
Reaction Steps
A mixture of 5 g of 4-(methylthio)benzoic acid (97%) and 30 mL of glacial acetic acid was formed. The mixture was cooled in a water bath containing a small amount of ice. To the mixture was added 8.5 g of 30% hydrogen peroxide gradually over one hour. No temperature rise was observed during the addition of the hydrogen peroxide. The reaction mixture was then heated for one and a half hours with the temperature ranging between 70° C. and 100° C. Heating was stopped and the reaction mixture was allowed to cool to room temperature. A solid was present in the reaction mixture. A solution of 3 g of sodium sulfite in 57 g of water was added to the reaction mixture. The solid was filtered from solution and was washed three times with cold deionized water. The solid was transferred to a watchglass and dried overnight. The dried product weighed 5.25 g which is a yield of 88.1% of the theoretical based upon the amount of the starting benzoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05364959 |
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| Source dataset | uspto-grants-1994_11 |
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| ORD ID | ord-2cedec505ebe4ddc8fe9707a5a94bedc |
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| Source note | uspto-grants-1994_11 |
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