HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Naphthaleneethanol → 4-Benzamido-1-[2-(2-naphthyl)ethyl]piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Naphthaleneethanol | HCID 73877 | — |
| Reactant | N-4-Piperidylbenzamide | HCID 118120 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 4-Benzamido-1-[2-(2-naphthyl)ethyl]piperidine | HCID 21430613 | — |
Reaction Steps
2-(2-Naphthyl)ethanol (3.44 g., 0.02 mole), 4-benzamidopiperidine (4.08 g., 0.02 mole) and Raney Nickel (W7 ca. 5 g.) were suspended in xylene (200 ml.) and the stirred mixture boiled under reflux for 16 hours. Liberated water was removed by means of a Dean and Stark apparatus. The mixture was filtered hot and evaporated to ca. 100 ml. The resulting yellow solution was stored until crystallisation was complete. The title compound was obtained as off-white needles (3.30 g.), m.p. 189°-191° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04029801 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-f0ae86a5d7d94fe7a08083e5cbbad43a |
| Source note | uspto-grants-1977_06 |