HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 4-Piperidinylbut-1-ene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Homoallyl bromide | HCID 21241 | — |
| Product | 4-Piperidinylbut-1-ene | HCID 4562282 | 93.4% |
Reaction Steps
A mixture of 1-bromo-3-butene (1.35 g, 10 mmol) and piperidine (1.70 g, 20 mmol) neat was refluxed under nitrogen atmosphere for 3 h. Cooled to RT, filtered and dissolved into ethyl ether (40 mL). Then solution was washed with water (2×30 mL) and dried over anhydrous Na2SO4, filtered and evaporated to dryness to yield 1.3 g (74.15%) oily 1-piperidyl-3-butene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07087757B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-2927bd8c3c9846bbb36c39855a81a50c |
| Source note | uspto-grants-2006_08 |