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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034644Generated: October 31, 2026

Tert-butyl trans-1-benzyl-4-methylpiperidin-3-ylcarbamate → trans-tert-Butyl (4-methylpiperidin-3-yl)carbamate

https://huagongshe.com/reaction/1034644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl trans-1-benzyl-4-methylpiperidin-3-ylcarbamateHCID 67045797—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Producttrans-tert-Butyl (4-methylpiperidin-3-yl)carbamateHCID 5793112895.5%

Reaction Steps

A mixture of tert-butyl trans-1-benzyl-4-methylpiperidin-3-ylcarbamate (0.64 g, 2.1 mmol) and 10% Pd/C (0.22 g, 0.21 mmol) in methanol (10 mL) was charged with 1 atmosphere hydrogen and stirred at room temperature for 18 hours. The catalyst was removed by filtration and washed with methanol (20 mL). The filtrate was concentrated in vacuo to give tert-butyl trans-4-methylpiperidin-3-ylcarbamate (0.43 g, 95%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08545897B2
Source datasetuspto-grants-2013_10
ORD IDord-b318b40a009a4f6e91d0d5cb4407d120
Source noteuspto-grants-2013_10