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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1923683Generated: November 2, 2026

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

https://huagongshe.com/reaction/1923683

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 numberUS08178131B2
Source datasetuspto-grants-2012_05
ORD IDord-39e90cf90e234a338d658ee88a0f3b78
Source noteuspto-grants-2012_05