HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 3,4-Dihydro-2,2-dioxo-3-methyl-1,2-benzoxathiin-8-ylsulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2,2-Dioxo-4-methyl-1,2-benzoxathiin-8-ylsulfonamide | HCID 23310797 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | 3,4-Dihydro-2,2-dioxo-3-methyl-1,2-benzoxathiin-8-ylsulfonamide | HCID 13592075 | — |
Reaction Steps
10.0 g of 2,2-dioxo-4-methyl-1,2-benzoxathiin-8-ylsulfonamide are dissolved in 200 ml of tetrahydrofuran and the solution is hydrogenated with hydrogen for 21/2 hours, in the presence of 2.0 g of 5% palladium on carbon catalyst, under a pressure of 4 bar and at a temperature of 40° C. After removal of the catalyst the solution is concentrated and the residue is crystallised from 120 ml of 70% aqueous ethanol, affording 9.0 g of 3,4-dihydro-2,2-dioxo-3-methyl-1,2-benzoxathiin-8-ylsulfonamide of m.p. 185°-186° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04560771 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-ae073cdc61814a02bfdf0686e00ab713 |
| Source note | uspto-grants-1985_12 |