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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034651Generated: November 2, 2026

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

https://huagongshe.com/reaction/1034651

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 numberUS08545897B2
Source datasetuspto-grants-2013_10
ORD IDord-42300988fe8e45d783a9e5ae5f1c3ff5
Source noteuspto-grants-2013_10