HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23919Generated: October 26, 2026
Methanesulfonic Acid → 1-(3,5-Dioxapiperidin-1-yl)sulphonyl-4-nitrobenzene
https://huagongshe.com/reaction/23919
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | 1,3,5-Trioxane | HCID 8081 | — |
| Reactant | 4-Nitrobenzenesulfonamide | HCID 22784 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(3,5-Dioxapiperidin-1-yl)sulphonyl-4-nitrobenzene | HCID 22024921 | 35% |
Reaction Steps
4-Nitrobenzenesulphonamide (2.02 g, 10 mmol) was added to a solution of 1,3,5-trioxane (1.96 g, 20 mmol) in acetic acid (5 ml). The mixture was cooled for 5 minutes ated methanesulphonic acid (10 ml) was added slowly. The mixture was then stirred at 35° C. for 20 minutes, cooled to 0° C., diluted with water and extracted with ethyl acetate. The combined extracts were washed twice with water and twice with 5% aqueous sodium hydrogen carbonate solution, then dried and the volatiles removed by evaporation. The residue was recrystallized from ethanol to give the title compound (955 mg, 35%). NMR: 4.87 (s, 2H), 5.30 (s, 4H), 8.20 (d, 2H), 8.42 (d, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06855719B1 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-8b51693c7334427b91306a3c319f4ad9 |
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| Source note | uspto-grants-2005_02 |
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