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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501839Generated: October 31, 2026

Ethyl 1-benzyl-4-(cyanomethyl)-3-oxopiperidine-4-carboxylate → Ethyl 4-(2-aminoethyl)-1-benzyl-3-hydroxypiperidine-4-carboxylate

https://huagongshe.com/reaction/1501839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 1-benzyl-4-(cyanomethyl)-3-oxopiperidine-4-carboxylateHCID 86709485—
CatalystPlatinum oxide (PtO)HCID 82844—
SolventAcetic acid methanolHCID 10129899—
ProductEthyl 4-(2-aminoethyl)-1-benzyl-3-hydroxypiperidine-4-carboxylateHCID 86709519—

Reaction Steps

Into a 10000-mL 4-necked round-bottom flask was placed a solution of ethyl 1-benzyl-4-(cyanomethyl)-3-oxopiperidine-4-carboxylate (180 g, 599.30 mmol) in acetic acid/methanol (1:1, 5.4 L) and platinum oxide (27 g, 118.90 mmol). The flask was then flushed and charged with hydrogen and stirred overnight at room temperature. After filtration under nitrogen through CELITE®, the filtrate was concentrated under vacuum to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206198B2
Source datasetuspto-grants-2015_12
ORD IDord-4582b30168db4c229d4ef8e76ec32a45
Source noteuspto-grants-2015_12