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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981298Generated: October 30, 2026

Ethyl trans-4-azido-3-methoxy-1-piperidinecarboxylate → Ethyl trans-4-amino-3-methoxy-1-piperidinecarboxylate

https://huagongshe.com/reaction/981298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl trans-4-azido-3-methoxy-1-piperidinecarboxylateHCID 13677848—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductEthyl trans-4-amino-3-methoxy-1-piperidinecarboxylateHCID 1367774797.4%

Reaction Steps

A mixture of 15.6 parts of ethyl trans-4-azido-3-methoxy-1-piperidinecarboxylate and 200 parts of methanol was hydrogenated at normal pressure and at room temperature with 2 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated in vacuo, yielding 13.8 parts (97.4%) of ethyl trans-4-amino-3-methoxy-1-piperidinecarboxylate as a residue (interm. 5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04990521
Source datasetuspto-grants-1991_02
ORD IDord-afed1b3cc59e414a9f5917e0bd69902c
Source noteuspto-grants-1991_02