HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 53925198, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-Methoxybenzaldehyde | HCID 31244 | — |
| Reactant | HCID 86748976 | HCID 86748976 | — |
| Product | HCID 53925198 | HCID 53925198 | — |
Reaction Steps
A mixture of 3,5-dinitro-p-methyltoluate (120.08 grams) from Example 1, p-anisaldehyde (68.08 grams), activated basic alumina oxide (150 mesh, 58 angstrom, 70.00 grams), and ethyl acetate (150.0 grams) was heated to reflux. Piperidine (15.3 grams) was added dropwise over 5 hours and the reaction held at reflux for another 6.5 hours. Upon cooling, a yellow crystalline product precipitated and was isolated by filtration. The crude product was recrystallized one time from concentrated ethyl acetate to recover 77.6 grams of bright yellow 2,6-dinitro-4- carbomethoxy-4'-methoxystilbene (4). The product was characterized by NMR and had a melting point of 141.5° to 143° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05489714 |
| Source dataset | uspto-grants-1996_02 |
| ORD ID | ord-754c091472b146b9a2bc67e3ba4320af |
| Source note | uspto-grants-1996_02 |