HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Benzeneethanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Phenylethane-1-sulfonyl chloride | HCID 2760374 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzeneethanesulfonamide | HCID 204808 | — |
Reaction Steps
A solution of 2-phenylethanesulfonyl chloride (40.94 g) in THF (250 ml) was cooled to −20° C. before it was treated with sat. aq. ammonia (50 ml). The brown suspension was stirred at rt for 16 h. The mixture was neutralised with aq. HCl and the organic solvent was evaporated. The remaining suspension was diluted with water and extracted four times with EA. The organic layers were combined and evaporated to give 2-phenyl-ethanesulfonic acid amide (33.06 g) as orange solid. 1H-NMR(300 MHz, CDCl3): 3.15–3.21(m, 2H), 3.38–3.45(m, 2H), 4.59(s br, 2H), 7.21–7.37(m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07091201B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-aefda4e42cde42d1b7ffd52f52e1272a |
| Source note | uspto-grants-2006_08 |