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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203715Generated: November 1, 2026

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

https://huagongshe.com/reaction/2203715

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 numberUS09365568B2
Source datasetuspto-grants-2016_06
ORD IDord-879923d8856042a683f826c2326a6177
Source noteuspto-grants-2016_06