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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49717Generated: October 30, 2026

Ethyl 3-(6-acetylamino-pyrid-3-yl)-but-2-enoate → (RS) ethyl 3-(6-acetylamino-pyrid-3-yl)-butanoate

https://huagongshe.com/reaction/49717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(6-acetylamino-pyrid-3-yl)-but-2-enoateHCID 69687042—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product(RS) ethyl 3-(6-acetylamino-pyrid-3-yl)-butanoateHCID 17946644—

Reaction Steps

A solution of (E/Z) ethyl 3-(6-acetylamino-pyrid-3yl)-but-2-enoate (27.3 g, Reference Example 22) in ethanol (500 mL) was hydrogenated (3bar hydrogen pressure) at 50° C. using 10% palladium on charcoal (1.0 g) as catalyst. After 48 h, the mixture was degassed, filtered through a pad of diatomaceous earth and the pad rinsed through with ethanol. The filtrate was evaporated to give the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706738B2
Source datasetuspto-grants-2004_03
ORD IDord-4097b70c76fb450caf839a728293046c
Source noteuspto-grants-2004_03