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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522679Generated: October 28, 2026

1,3,5-Trioxane → 6-Nitro-3,4(1H)-dihydro-2,3-benzothiazine 2,2-dioxide

https://huagongshe.com/reaction/522679

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3,5-TrioxaneHCID 8081—
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant(4-Nitrophenyl)methanesulfonamideHCID 2755281—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
Product6-Nitro-3,4(1H)-dihydro-2,3-benzothiazine 2,2-dioxideHCID 59595723%

Reaction Conditions

Temperature35 °C

Reaction Steps

To a mixture of (4-nitrophenyl)methanesulfonamide (864 mg, 4.0 mmol) and s-trioxane (120 mg, 4.0 mmol) in 1,2-dichoroethane (10 mL) was added trifluoromethanesulfonic acid (1.5 mL), followed by the addition of trifluoromethanesulfonic anhydride (1.5 mL, 4.0 mmol). The reaction mixture was stirred at 35° C. for 2 hours and refluxed overnight. The mixture was then diluted with dichloromethane (100 mL) and washed with water (100 mL) and brine (50 mL). The solvents were evaporated and the residue was purified by Prep-HPLC to give 6-nitro-3,4-dihydro-1H-benzo[d][1,2]thiazine 2,2-dioxide (210 mg, 23%) as a gray solid. MS (ES+) C8H8N2O4S requires: 228, found: 229 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334263B2
Source datasetuspto-grants-2016_05
ORD IDord-04ed11a5cc7b4f0082559b7cfe67718d
Source noteuspto-grants-2016_05