Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791179Generated: October 27, 2026

Pyridine → Ethyl 3-acetamido-2-oxopentanoate

https://huagongshe.com/reaction/1791179

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 tetrahydrofuran 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 numberUS07074790B2
Source datasetuspto-grants-2006_07
ORD IDord-6e9da760204a424b95349e789bfbea5b
Source noteuspto-grants-2006_07