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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026542Generated: November 1, 2026

tert-butyl 4-{[(2R)-2-(benzyloxy)propanoyl]amino}piperidine-1-carboxylate → tert-butyl 4-{[(2R)-2-hydroxypropanoyl]amino}piperidine-1-carboxylate

https://huagongshe.com/reaction/1026542

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 4-{[(2R)-2-(benzyloxy)propanoyl]amino}piperidine-1-carboxylateHCID 52331793—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
Producttert-butyl 4-{[(2R)-2-hydroxypropanoyl]amino}piperidine-1-carboxylateHCID 68500407100.1%

Reaction Steps

At room temperature, to a methanol solution (200 ml) of tert-butyl 4-{[(2R)-2-(benzyloxy)propanoyl]amino}piperidine-1-carboxylate (6.90 g) was added 10% palladium carbon (2.03 g), followed by stirring overnight under a hydrogen atmosphere. The reaction solution was filtered through Celite, and then concentrated under reduced pressure to afford tert-butyl 4-{[(2R)-2-hydroxypropanoyl]amino}piperidine-1-carboxylate (5.19 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729095B2
Source datasetuspto-grants-2014_05
ORD IDord-6504e2b6ee51466a8d70bdf03f882fda
Source noteuspto-grants-2014_05