HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 4-[(1-Benzyl-4-piperidinyliden)acetyl]aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | N-t-butoxycarbonyl-4-[(1-benzyl-4-piperidinyliden)acetyl]aniline | HCID 19968896 | — |
| Reactant | Sodium methanolate methanol | HCID 23694274 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-[(1-Benzyl-4-piperidinyliden)acetyl]aniline | HCID 19968936 | 75% |
Reaction Steps
4.12 g of N-t-butoxycarbonyl-4-[(1-benzyl-4-piperidinyliden)acetyl]aniline was added to 50 ml of chloroform, and then 10 ml of trifluoroacetic acid was added thereto. The mixture was stirred at room temperature for 4 hours. After the reaction, the reaction mixture was condensed under reduced pressure, and the residue was dissolved in chloroform. Then, the solution was neutralized by adding a 28% sodium methylate·methanol solution thereto. The residue obtained by condensation under reduced pressure was applied to silica gel column chromatography to obtain 2.33 g of the title compound as bluish green powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05610303 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-dba69cfb462f4624832458f705ffa6ef |
| Source note | uspto-grants-1997_03 |