Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655760Generated: October 27, 2026

Ethyl (3S,4R)-4-{[(benzyloxy)carbonyl]amino}-3-ethoxypiperidine-1-carboxylate → Ethyl (3S,4R)-4-amino-3-ethoxypiperidine-1-carboxylate

https://huagongshe.com/reaction/655760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl (3S,4R)-4-{[(benzyloxy)carbonyl]amino}-3-ethoxypiperidine-1-carboxylateHCID 58066116—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductEthyl (3S,4R)-4-amino-3-ethoxypiperidine-1-carboxylateHCID 5423747789.62%

Reaction Steps

Ethyl (3S,4R)-4-{[(benzyloxy)carbonyl]amino}-3-ethoxypiperidine-1-carboxylate (Intermediate 23, 2.4 g, 6.87 mmol) was dissolved in methanol (150 mL) and hydrogenated over 10% palladium on carbon (1.5 g) under 50 psi of hydrogen pressure for 2 h at room temperature. The reaction mixture was then filtered through a celite bed and the filtrate was concentrated under reduced pressure to yield 1.33 g (89.62%) of Ethyl (3S,4R)-4-amino-3-ethoxypiperidine-1-carboxylate as liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071605B2
Source datasetuspto-grants-2011_12
ORD IDord-06ee2082ea1c45aaa6f426e301b7cda4
Source noteuspto-grants-2011_12