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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664810Generated: November 2, 2026

Ethanol → 4-(((Benzyloxy)carbonyl)amino)-1-(tert-butoxycarbonyl)piperidine-4-carboxylic acid

https://huagongshe.com/reaction/1664810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactanttert-Butyl 4-(((benzyloxy)carbonyl)amino)-4-carbamoylpiperidine-1-carboxylateHCID 10714606—
CatalystPalladiumHCID 23938—
Product4-(((Benzyloxy)carbonyl)amino)-1-(tert-butoxycarbonyl)piperidine-4-carboxylic acidHCID 2756640—

Reaction Steps

Palladium (10% on carbon; 210 mg) was added to a solution of tert-butyl 4-(aminocarbonyl)-4-{[(benzyloxy)carbonyl]amino}piperidine-1-carboxylate (0.43 g, 1.14 mmol) in ethanol (20 mL). The reaction vessel was evacuated and back-filled with nitrogen (3×), then back-filled with hydrogen (1 atm). After 18 h, the mixture was filtered and concentrated to give the title compound (290 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039460B2
Source datasetuspto-grants-2011_10
ORD IDord-89fadd86f4d449e59f14afb14ccc9107
Source noteuspto-grants-2011_10