HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 4-(1-Acetylpiperidin-4-yl)benzenesulphonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 4-(1-Acetylpiperidin-4-yl)benzenesulphonyl chloride | HCID 20039820 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(1-Acetylpiperidin-4-yl)benzenesulphonamide | HCID 20039833 | — |
Reaction Steps
The product of (i) above (21.0 g) was added portionwise to a stirred mixture of concentrated aqueous ammonia solution (160 ml) and ethanol (160 ml). The mixture was warmed at 35° until solution was complete and then evaporated. The residue was triturated with water and the solid was filtered off and dried to give the title compound, (18.0 g), m.p. 196°-197° (from ethanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04835165 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-72a4f3b0303c4c06ac9a418e5d4a246f |
| Source note | uspto-grants-1989_05 |