HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Toluenesulfonamide → 2,5-Ditosyl-1,2,3,4,5,6-hexahydropyrrolo[3,4-c]pyrrole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Toluenesulfonamide | HCID 6269 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1,4-Dibromo-2,3-bis(bromomethyl)-2-butene | HCID 35343 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,5-Ditosyl-1,2,3,4,5,6-hexahydropyrrolo[3,4-c]pyrrole | HCID 15192252 | 54.1% |
Reaction Steps
30 g of tetrakis (bromomethyl)ethylene and 30 g of p-toluene sulfonamide were dissolved in 400 ml of dimethylformamide. 150 g of potassium carbonate anhydride (or 50% sodium hydride 17 g) was added and then stirred at room temperature for 24 hours. Thereafter, this reaction mixture was distilled under vacuum to remove solvents. By adding 30 ml of water and 100 ml of ethylacetate, 17 g of the title compound was obtained as pale yellow powder (yield 50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05089621 |
| Source dataset | uspto-grants-1992_02 |
| ORD ID | ord-f03b5ab59fc34e3d83f05a355149e801 |
| Source note | uspto-grants-1992_02 |