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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1923672Generated: November 1, 2026

HCID 67045806, compound → HCID 58195431, compound

https://huagongshe.com/reaction/1923672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67045806HCID 67045806—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 58195431HCID 58195431100.4%

Reaction Steps

A mixture of tert-butyl trans-1-benzyl-4-methoxypiperidin-3-ylcarbamate (1.37 g, 4.28 mmol) and 10% Pd/C (0.46 g, 0.43 mmol) in MeOH (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-methoxypiperidin-3-ylcarbamate (0.99 g, 100%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178131B2
Source datasetuspto-grants-2012_05
ORD IDord-7a2d55776dfc48e1a2ce34e6efa8671b
Source noteuspto-grants-2012_05