HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidin-3-ylmethanol → 1-(4-Acetylbenzenesulfonyl)-3-piperidinemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidin-3-ylmethanol | HCID 107308 | — |
| Reactant | 4-Acetylbenzenesulfonyl chloride | HCID 266418 | — |
| Reactant | Sodium 4-acetylbenzenesulphonate | HCID 23668814 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(4-Acetylbenzenesulfonyl)-3-piperidinemethanol | HCID 4985981 | — |
Reaction Steps
The damp 4-acetylbenzenesulfonyl chloride from 100 g. of sodium 4-acetylbenzenesulfonate is added to a solution of 114 g. of 3-piperidinemethanol in 900 ml. of water. The mixture is stirred at room temperature for 16 hours, cooled, and the precipitate for 1-(4-acetylbenzenesulfonyl)-3-piperidinemethanol collected by filtration, washed with water and dried; m.p. 104°-106° C. after crystallization from aqueous ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04101661 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-0d6f56a8beb046c6a4ee9bb05c5b6259 |
| Source note | uspto-grants-1978_07 |