HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 1-[4-(1-Piperidinylsulfonyl)phenyl]ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 4-Acetylbenzenesulfonyl chloride | HCID 266418 | — |
| Reactant | Sodium 4-acetylbenzenesulphonate | HCID 23668814 | — |
| Product | 1-[4-(1-Piperidinylsulfonyl)phenyl]ethanone | HCID 750364 | — |
Reaction Steps
The damp 4-acetylbenzenesulfonyl chloride from 100 g. of sodium 4-acetylbenzenesulfonate is added to a stirred solution of 500 ml. of 50% aqueous piperidine. The mixture is stirred at room temperature for 16 hours, cooled, and the precipitated 1-(4-acetylbenzenesulfonyl)-piperidine removed by filtration, washed with water and dried; m.p. 113°-114° C. after crystallization from 2-propanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04137408 |
| Source dataset | uspto-grants-1979_01 |
| ORD ID | ord-7ecd2e718f494850b7540acefdd49e6d |
| Source note | uspto-grants-1979_01 |