HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indole → HCID 21512049, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indole | HCID 798 | — |
| Reactant | Phosphoric Acid | HCID 1004 | — |
| Reactant | N-Acetyl-4-piperidone | HCID 122563 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 21512049 | HCID 21512049 | — |
Reaction Steps
A starting compound of the formula II may also be obtained by reacting an indole of the formula IV in a mixture of glacial acetic acid and phosphoric acid with the equivalent quantity of N-acetyl-4-piperidone, preferably at room temperature. The corresponding 4-indolyl-1-acetyl-1,2,5,6-tetrahydropyridine is thus obtained, which is then hydrogenated in conventional manner in the presence of palladium/coal at room temperature and atmospheric pressure to form the corresponding piperidine derivative; the latter is subsequently hydrolized in a mixture of a lower alkanol and aqueous 50% potassium hydroxide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03980658 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-36f9bb7e93a14a59a508b09597e5f251 |
| Source note | uspto-grants-1976_09 |