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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19463Generated: October 29, 2026

1-Benzyl-4-(N-Boc-amino)piperidine → 4-(N-Boc-amino)piperidine

https://huagongshe.com/reaction/19463

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-(N-Boc-amino)piperidineHCID 4438618—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-(N-Boc-amino)piperidineHCID 72383391%

Reaction Steps

A solution of 1-benzyl-4-tertbutyloxycarbonylaminopiperidine 5 (7.95 g; 27.4 mmol) in 120 ml of MeOH is poured into a hydrogenation reactor. 10% Pd/c-based catalyst is added (1.46 g; 1.38 mmol) and the mixture is subjected to a hydrogen pressure of 3.5 bars (50 psi) for 24 hours in a Parr type shaker. After filtration on celite and washing with methanol, the medium is concentrated in order to produce 4.98 g (Yield=91%) of product in the form of white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745413B2
Source datasetuspto-grants-2010_06
ORD IDord-7fbbc4b12374417a9e72e3284df826eb
Source noteuspto-grants-2010_06