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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
Reactant1,3,5-TrioxaneHCID 8081—
Reactant4-NitrobenzenesulfonamideHCID 22784—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product1-(3,5-Dioxapiperidin-1-yl)sulphonyl-4-nitrobenzeneHCID 2202492135%

Reaction Conditions

Temperature35 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855719B1
Source datasetuspto-grants-2005_02
ORD IDord-8b51693c7334427b91306a3c319f4ad9
Source noteuspto-grants-2005_02