HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → N-allyl-N-(2-bromo-5-nitrophenyl)methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | N-(2-bromo-5-nitrophenyl)methanesulfonamide | HCID 18789758 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | N-allyl-N-(2-bromo-5-nitrophenyl)methanesulfonamide | HCID 18789667 | 99.8% |
Reaction Steps
Allyl bromide (1.36 g, 11.25 mmol) was added to a mixture of N-(2-bromo-5-nitrophenyl)methanesulfonamide (1.66 g, 5.62 mmol) and cesium carbonate (5.49 g, 16.86 mmol) in methylethylketone (20 ml). The mixture was heated to reflux for 2 hr. The mixture was cooled and poured onto water. The product was extracted into ethyl acetate (2×75 ml) and the extracts were dried (anhydrous MgSO4) and concentrated to provide 1.88 g of N-allyl-N-(2-bromo-5-nitrophenyl)methanesulfonamide which required no purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05952362 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-d399b87b3b4a454f911de8126ce0853f |
| Source note | uspto-grants-1999_09 |