HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 11-(Piperidin-1-yl)undecan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 11-Bromo-1-undecanol | HCID 74163 | — |
| Reactant | Piperidine, hydrobromide (1:1) | HCID 203244 | — |
| Product | 11-(Piperidin-1-yl)undecan-1-ol | HCID 3122283 | 96.3% |
Reaction Steps
11-Bromoundecanol (11.00 g., 43.79 mmole) was dissolved in 100 ml. of piperidine and heated at reflux temperature for 18 hours. The reaction mixture was allowed to cool and most of the precipitated piperidine hydrobromide was removed by filtration. The excess piperidine is removed by simple distillation and the resultant solid residue is recrystallized from ethanol and water. After drying, 10.78 g. (96.3% yield) of 1-hydroxy-11-(N-piperidyl)undecane was obtained . m.p. 62°-65° C., 1H-NMR (200 MHz, CDCl3) δ=1.2-1.7 ppm, m, 24H; 2.10, broad s, 1H; 2.20-2.45, m, 6H; 3.63, t, 2H.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05149524 |
| Source dataset | uspto-grants-1992_09 |
| ORD ID | ord-41723e7074b44283811eb5dd0fb97725 |
| Source note | uspto-grants-1992_09 |