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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181511Generated: November 4, 2026

1-Benzyl-4-(N-tert-butoxycarbonyl-N-isopropylamino)piperidine → tert-butyl N-(piperidin-4-yl)-N-(propan-2-yl)carbamate

https://huagongshe.com/reaction/1181511

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-(N-tert-butoxycarbonyl-N-isopropylamino)piperidineHCID 67428416—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Producttert-butyl N-(piperidin-4-yl)-N-(propan-2-yl)carbamateHCID 5098657399%

Reaction Steps

A solution of 1-benzyl-4-(N-tert-butoxycarbonyl-N-isopropylamino)piperidine (79.0 g, 0.24 mol) in ethanol (140 mL) was flushed with nitrogen for 15 minutes. This solution was then added to a 2 L Parr flask containing a mixture of 10% palladium on carbon (15.8 g; ca. 50% wt. water) in ethanol (100 mL), which solution had been flushed with nitrogen for 15 minutes. This reaction mixture was placed on a Parr Shaker under hydrogen at 50 psi for 24 hours. The reaction mixture was filtered through a pad of Celite and the Celite washed with ethanol. The filtrate was then concentrated in vacuo to afford 57.0 g of the title intermediate as a white solid (>99% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285564B2
Source datasetuspto-grants-2007_10
ORD IDord-023f735e6bf5416ca0f2f4f3a198eb17
Source noteuspto-grants-2007_10