HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746288Generated: October 30, 2026
Triethylamine → 3-Methyl-8-sulfamoyl-2,2-dioxo-1,2-benzoxathiine
https://huagongshe.com/reaction/746288
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-Bromo-2,2-dioxo-3-methyl-1,2-benzoxathiin-8-ylsulfonamide | HCID 13592073 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Methyl-8-sulfamoyl-2,2-dioxo-1,2-benzoxathiine | HCID 13592074 | 75.1% |
Reaction Steps
120 g of 6-bromo-2,2-dioxo-3-methyl-1,2-benzoxathiin-8-ylsulfonamide are dissolved in 2.4 liters of tetrahydrofuran and the solution is hydrogenated with hydrogen for 40 minutes, in the presence of 41.3 g of triethylamine and 12.0 g of 5% palladium on carbon catalyst, under normal pressure and in the temperature range from 20° to 25° C. The mixture is filtered, the filtrate is concentrated, and the residue is taken up in 1300 ml of hot 90% aqueous ethanol. The insoluble constituents are separated and the solution is cooled to 0° C. The precipitate is separated and dried, affording 70 g of 2,2-dioxo-3-methyl-1,2-benzoxathiin-8-ylsulfonamide of m.p. 204°-205° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04603211 |
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| Source dataset | uspto-grants-1986_07 |
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| ORD ID | ord-892b0c62711c44559d00a55d318f0e3e |
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| Source note | uspto-grants-1986_07 |
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