HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (E)-4-[3-(1-benzylpiperidin-4-yl)propenoyl]aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | (E)-4-[3-(1-benzylpiperidin-4-yl)propenoyl]nitrobenzene | HCID 70279862 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | (E)-4-[3-(1-benzylpiperidin-4-yl)propenoyl]aniline | HCID 19968908 | — |
Reaction Steps
1.27 g of (E)-4-[3-(1-benzylpiperidin-4-yl)propenoyl]nitrobenzene was added to a mixed solution of 10 ml of acetic acid and 2 ml of hydrochloric acid, and then 1.38 g of stannous chloride was added thereto under ice cooling. The mixture was stirred for 24 hours. During the reaction, 0.69 g of stannous chloride was further added twice. After completion of the reaction, the reaction mixture was condensed under reduced pressure to obtain 5.50 g of a crude product of the title compound. This was used without purification for the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05610303 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-f358fc38bacd4c36af71ca2eff7151e2 |
| Source note | uspto-grants-1997_03 |