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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7536Generated: October 26, 2026

Pyridine → Ethyl 3-acetamido-2-oxopentanoate

https://huagongshe.com/reaction/7536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthoxalyl chlorideHCID 20884—
Reactant2-(Acetylamino)butanoic acidHCID 306107—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-acetamido-2-oxopentanoateHCID 21935058—

Reaction Steps

9.2 g (63.4 mmol) 2-(acetylamino)butanoic acid are suspended in 120 ml tetrahydro-furane and heated to reflux together with 15.0 g (190 mmol) pyridine and a bit of N,N-dimethylaminopyridine. While heating at reflux, 17.3 g (127 mmol) ethyl chloro(oxo)acetate are added dropwise. The reaction mixture is heated at reflux until no more evolution of gas can be observed. After cooling down to room temperature, the reaction mixture is added to ice water and the organic phase extracted with ethyl acetate. The dried organic phase is evaporated to dryness in vacuo, dissolved in ethanol and the solution directly used for the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087605B2
Source datasetuspto-grants-2006_08
ORD IDord-104f1562f4d446dfad9da36770411e4b
Source noteuspto-grants-2006_08