HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → N-[1-(phenylmethyl)-4-piperidinylidene]-3-pyridinamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3-Aminopyridine | HCID 10009 | — |
| Reactant | 1-Benzyl-4-piperidone | HCID 19220 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-[1-(phenylmethyl)-4-piperidinylidene]-3-pyridinamine | HCID 10706822 | — |
Reaction Steps
A mixture of 19 parts of 1-(phenylmethyl)-4-piperidinone, 11.8 parts of 3-pyridinamine, 120 parts of methylbenzene and a small volume of 4-methylbenzenesulfonic acid is stirred and refluxed for 5 hours. (The reaction vessel is provided with reflux-condensor and water-separator). After the calculated amount of water is separated, the solvent is evaporated. The oily residue is dissolved in 800 parts of 2,2'-oxybispropane and evaporated again, yielding 27 parts of N-[1-(phenylmethyl)-4-piperidinylidene]-3-pyridinamine as a yellow-brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04225606 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-699b85be31244c90849a82aab9a3aa96 |
| Source note | uspto-grants-1980_09 |