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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787572Generated: October 30, 2026

Ethanol → Ethyl 3-oxo-3-(pyridin-2-yl)propanoate

https://huagongshe.com/reaction/1787572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantEthyl AcetateHCID 8857—
ReactantEthyl 2-pyridinecarboxylateHCID 17307—
ReactantSodium ethoxideHCID 2723922—
SolventTolueneHCID 1140—
ProductEthyl 3-oxo-3-(pyridin-2-yl)propanoateHCID 273646191%

Reaction Conditions

Temperature90 °C

Reaction Steps

Stir a mixture of sodium ethoxide (360 g, 5.29 mol), toluene (4 L), ethanol (18 mL, 0.265 mol), and ethyl acetate (1.04 L, 10.6 mol) in a 22 L flask equipped with a reflux condenser, nitrogen inlet, and mechanical stirrer. Stir for 1 h as the mixture warms to 26° C. Add pyridine-2-carboxylic acid ethyl ester (Fluka; 400 g, 2.65 mol) and heat the mixture to reflux (90° C.) for 18 h. Cool the mixture to room temperature, dilute with toluene (8 L), wash with water (6 L), and separate the layers. Acidify the aqueous layer to pH 5 with glacial acetic acid. Extract with ethyl acetate (2×4 L), dry the combined organic layers (sodium sulfate), filter, and concentrate in vacuo to yield 466 g (91%) the subtitled compound as a dark oil in 93% purity by HPLC analysis. MS (ES) m/z=194 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511056B2
Source datasetuspto-grants-2009_03
ORD IDord-553d874a2d1b469fb510ce29b1584ada
Source noteuspto-grants-2009_03