HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-[3-(1-Benzylpiperidin-4-yl)propanoyl]aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | (E)-4-[3-(1-benzylpiperidin-4-yl)propenoyl]nitrobenzene | HCID 70279862 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Platinum oxide (PtO) | HCID 82844 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-[3-(1-Benzylpiperidin-4-yl)propanoyl]aniline | HCID 19968919 | 37.5% |
Reaction Steps
2.00 g of (E)-4-[3-(1-benzylpiperidin-4-yl)propenoyl]nitrobenzene was added to a mixed solvent of 30 ml of ethanol and 5 ml of acetic acid, and then 0.20 g of platinum oxide was added thereto. Thereafter, the mixture was stirred in a hydrogen stream at room temperature for 7.5 hours. After the reaction, the catalyst was removed by filtration, and the filtrate was condensed under reduced pressure. The obtained residue was applied to silica gel column chromatography to obtain 0.69 g of the title compound as pale yellow crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05610303 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-ae05ad79f9eb4e99b49d5b851aab7b27 |
| Source note | uspto-grants-1997_03 |