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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171599Generated: November 1, 2026

HCID 68766842, compound → HCID 68769736, compound

https://huagongshe.com/reaction/1171599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68766842HCID 68766842—
ReactantHCID 178418361HCID 178418361—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
ProductHCID 68769736HCID 68769736—

Reaction Steps

A mixture of (3R,4S)-tert-butyl 3-(hydroxymethyl)-4-((S)-1-phenylethylamino)piperidine-1-carboxylate (38 g, 113.6 mMol) and Pd(OH)2 (5 g) were stirred in methanol (250 mL) at rt under 50 psi hydrogen. After overnight stirring, the reaction mixture was filtered through Celite. The solution was concentrated to get the desired product, (3R,4S)-tert-butyl 4-amino-3-(hydroxymethyl)piperidine-1-carboxylate as a pale oil (quantitative yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829571B2
Source datasetuspto-grants-2010_11
ORD IDord-be9d9deb85f54e69a534c1948920c7f8
Source noteuspto-grants-2010_11