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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787544Generated: October 29, 2026

Nicotinic Acid → Ethyl 3-oxo-3-(pyridin-3-yl)propanoate

https://huagongshe.com/reaction/1787544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNicotinic AcidHCID 938—
ReactantImidazolateHCID 3386966—
ReactantPotassium ethyl malonateHCID 3446434—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
ReactantMagnesium ChlorideHCID 5360315—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-oxo-3-(pyridin-3-yl)propanoateHCID 22219749.6%

Reaction Steps

To a suspension of nicotinic acid 5.00 g (40.6 mmol) in tetrahydrofuran 50 mL was added carbonyl diimidazole 9.76 g (60.9 mmol) at 5° C. and stirred at room temperature for 1 hour. In a separate flask, a suspension of MgCl2 4.64 g (48.7 mmol) and ethyl malonate potassium salt 10.37 g (60.92 mmol) in tetrahydrofuran 50 mL was stirred at 50° C. for 4 hours. To this suspension was added the aforementioned imidazolide solution at room temperature and stirred for 12 hours. The reaction was quenched by the addition of water and extracted into ethyl acetate. The organic layer was washed by brine, dried over MgSO4, filtrated and the solvent was evaporated. Silica gel chromatography (n-hexane/AcOEt=2/1) afforded the titla compound 3.89 g as pale yellow oil. Yield 49.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511041B2
Source datasetuspto-grants-2009_03
ORD IDord-09d853b9f24644af997a1a56318ef3e7
Source noteuspto-grants-2009_03