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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275233Generated: October 31, 2026

N-Benzyloxycarbonyl-3-(4-acetoxy-4-phenylpiperidin-1-yl)propylamine → 3-(4-Acetoxy-4-phenylpiperidin-1-yl)propylamine

https://huagongshe.com/reaction/1275233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Benzyloxycarbonyl-3-(4-acetoxy-4-phenylpiperidin-1-yl)propylamineHCID 22993462—
CatalystPalladiumHCID 23938—
SolventAmmoniaHCID 222—
SolventMethanolHCID 887—
Product3-(4-Acetoxy-4-phenylpiperidin-1-yl)propylamineHCID 1077885299.6%

Reaction Steps

A mixture of N-benzyloxycarbonyl-3-(4-acetoxy-4-phenylpiperidin-1-yl)propylamine (3.0 g, 7.3 mmol) and 10% Pd-C (0.3 g) in 1M ammonia in methanol(50 mL) was hydrogenated at 70 psi at room temperature for 4 h. The catalyst was removed by filtration and the solvent was evaporated to leave the product as a viscous oil (2.01 g, 99%), the 1H-NMR showed it to be very pure and was used in the next step without any purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06159990
Source datasetuspto-grants-2000_12
ORD IDord-1662d06c2ece48718c3f2d02a5ba54b8
Source noteuspto-grants-2000_12