Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976149Generated: October 25, 2026

1-Benzyl-4-piperidone → N-t-butoxycarbonyl-4-[(1-benzyl-4-hydroxypiperidin-4-yl)acetyl]aniline

https://huagongshe.com/reaction/976149

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-piperidoneHCID 19220—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyl (4-acetylphenyl)carbamateHCID 15373979—
ReactantHCID 178446069HCID 178446069—
SolventTetrahydrofuranHCID 8028—
ProductN-t-butoxycarbonyl-4-[(1-benzyl-4-hydroxypiperidin-4-yl)acetyl]anilineHCID 1996890665.4%

Reaction Steps

30 ml of tetrahydrofuran was added to 2.00 g of N-t-butoxycarbonyl-4-acetylaniline, and 8.8 ml of a 1.7M t-butyl lithium·pentane solution was added thereto under an argon stream at -78° C. Then, 1.41 g of 1-benzyl-4-piperidone was dissolved in 20 ml of tetrahydrofuran, and the solution was added dropwise. After stirring for 2 hours, a saturated ammonium chloride aqueous solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate and dried over anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure, and the obtained residue was applied to silica gel column chromatography to obtain 2.07 g of the title compound as white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05610303
Source datasetuspto-grants-1997_03
ORD IDord-9defd28aaa69446d8e4abf7af16a5a38
Source noteuspto-grants-1997_03