HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 2-Vinylpyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 21315534 | HCID 21315534 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Vinylpyridine | HCID 7521 | — |
| Product | 4-Piperidinopyridine | HCID 76002 | — |
Reaction Steps
To 28.1 parts of this 1-[2-(2-pyridyl)ethyl]-4-cyanopyridinium chloride hydrochloride in 150 parts water was added 24 parts of piperidine, and the resulting mixture stirred for 2.5 hours at ambient temperature. 300 parts of 40% sodium hydroxide was added, and the reaction heated to 100° C. for two hours, cooled, and the organic layer separated. Distillation of the organic layer gave 15 parts 4-piperidinopyridine and 10 parts 2-vinylpyridine which was subsequently recycled for use in preparing more pyridylethyl salts.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04158093 |
| Source dataset | uspto-grants-1979_06 |
| ORD ID | ord-7fc8db00f2d342e880e026bf796c2cbf |
| Source note | uspto-grants-1979_06 |