HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 69497341, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 57373319 | HCID 57373319 | — |
| Product | HCID 69497341 | HCID 69497341 | — |
Reaction Steps
A mixture of 6-acetamido-2-(N,N-dimethylaminomethylidene)-1-tetralone (11 g) obtained in Example 41-1) and piperidine (100 ml) was refluxed with heating for 24 hours. After excess piperidine was distilled out under reduced pressure, the resulting residue was crystallized using tetrahydrofuran-isopropyl ether to give 6-acetamido-2-(1-piperidinylmethylidene)-1-tetralone (7 g) as a light yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07115750B1 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-0d72a695ffdf4f63b078eb674369d302 |
| Source note | uspto-grants-2006_10 |