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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3,5-Trioxane | HCID 8081 | — |
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | (4-Nitrophenyl)methanesulfonamide | HCID 2755281 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Nitro-3,4(1H)-dihydro-2,3-benzothiazine 2,2-dioxide | HCID 595957 | 23% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09334263B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-04ed11a5cc7b4f0082559b7cfe67718d |
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| Source note | uspto-grants-2016_05 |
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