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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203722Generated: November 1, 2026

Tert-butyl trans-1-benzyl-4-cyclopropylpiperidin-3-ylcarbamate → Tert-butyl-trans-4-cyclopropylpiperidin-3-ylcarbamate

https://huagongshe.com/reaction/2203722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl trans-1-benzyl-4-cyclopropylpiperidin-3-ylcarbamateHCID 67045345—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductTert-butyl-trans-4-cyclopropylpiperidin-3-ylcarbamateHCID 86652140100%

Reaction Steps

A mixture of tert-butyl trans-1-benzyl-4-cyclopropylpiperidin-3-ylcarbamate (1.20 g, 3.63 mmol) and 10% Pd/C (0.39 g, 0.36 mmol) in methanol (20 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-cyclopropylpiperidin-3-ylcarbamate (0.87 g, 100%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365568B2
Source datasetuspto-grants-2016_06
ORD IDord-96448c64d7b2438d954d8527e6e58ea9
Source noteuspto-grants-2016_06