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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976151Generated: October 29, 2026

Trifluoroacetic acid → 4-[(1-Benzyl-4-piperidinyliden)acetyl]aniline

https://huagongshe.com/reaction/976151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantN-t-butoxycarbonyl-4-[(1-benzyl-4-piperidinyliden)acetyl]anilineHCID 19968896—
ReactantSodium methanolate methanolHCID 23694274—
SolventChloroformHCID 6212—
Product4-[(1-Benzyl-4-piperidinyliden)acetyl]anilineHCID 1996893675%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05610303
Source datasetuspto-grants-1997_03
ORD IDord-dba69cfb462f4624832458f705ffa6ef
Source noteuspto-grants-1997_03