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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408125Generated: October 31, 2026

Benzyl 3-((tert-butoxycarbonyl)amino)-3-methylpiperidine-1-carboxylate → Tert-butyl (3-methylpiperidin-3-yl)carbamate

https://huagongshe.com/reaction/408125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 3-((tert-butoxycarbonyl)amino)-3-methylpiperidine-1-carboxylateHCID 60205232—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductTert-butyl (3-methylpiperidin-3-yl)carbamateHCID 1969147372.3%

Reaction Steps

Benzyl 3-(tert-butoxycarbonylamino)-3-methylpiperidine-1-carboxylate (1.4 g, 4.0 mmol) and 10% Pd/C (0.21 g, 0.2 mmol) in MeOH (20 mL) were stirred under H2 atmosphere (1 atm) for 1 hour. The catalyst was removed by filtration and washed with methanol. The filtrate was concentrated to give tert-butyl 3-methylpiperidin-3-ylcarbamate (0.62 g, 72% yield) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08758830B2
Source datasetuspto-grants-2014_06
ORD IDord-053bea94291648009071240d6e78e6d4
Source noteuspto-grants-2014_06