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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610436Generated: November 2, 2026

Water → Ethyl 3-(6-chloropyridin-3-yl)-3-oxopropanoate

https://huagongshe.com/reaction/1610436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant6-Chloronicotinic acidHCID 79222—
ReactantHCID 178472271HCID 178472271—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-(6-chloropyridin-3-yl)-3-oxopropanoateHCID 10421283116.8%

Reaction Steps

To a solution of 6-chloro-3-pyridinecarboxylic acid (10 g, 63.5 mmol) in tetrahydrofuran (150 ml) was added 1,1′-carbonylbis-1H-imidazole (11.3 g, 69.8 mmol), and the mixture was heated under reflux for 30 min. The reaction solution was cooled and monoethyl malonate magnesium salt (10 g, 34.9 mmol) was added. The mixture was stirred at room temperature for 30 min. To the reaction solution was added water (200 ml) and the mixture was extracted with ethyl acetate (200 ml×2). The extract was washed with saturated brine, dried over anhydrous magnesium sulfate and evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1) to give ethyl 3-(6-chloro-3-pyridyl)-3-oxopropionate (9.28 g, 64%) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982348B2
Source datasetuspto-grants-2006_01
ORD IDord-69d5a2367eb744029f6caca86e8aed76
Source noteuspto-grants-2006_01