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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19464Generated: October 25, 2026

tert-Butyl ((1-benzylpiperidin-4-yl)methyl)carbamate → Tert-butyl (piperidin-4-ylmethyl)carbamate

https://huagongshe.com/reaction/19464

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl ((1-benzylpiperidin-4-yl)methyl)carbamateHCID 2824066—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductTert-butyl (piperidin-4-ylmethyl)carbamateHCID 723429100%

Reaction Steps

A solution of 1-benzyl-4-tertbutyloxycarbonylaminomethylpiperidine 8 (4.79 g; 15.7 mmol) in 120 ml of MeOH is poured into a hydrogenation reactor. The 10% Pd/C-based catalyst is added (0.872 g; 0.82 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 3.36 g (Yield=100%) 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-389f564054af4404af46e958b7bcb7da
Source noteuspto-grants-2010_06