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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nicotinic Acid | HCID 938 | — |
| Reactant | Imidazolate | HCID 3386966 | — |
| Reactant | Potassium ethyl malonate | HCID 3446434 | — |
| Reactant | Bis-(1H-imidazol-2-YL)-methanone | HCID 5250894 | — |
| Reactant | Magnesium Chloride | HCID 5360315 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 3-oxo-3-(pyridin-3-yl)propanoate | HCID 222197 | 49.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07511041B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-09d853b9f24644af997a1a56318ef3e7 |
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| Source note | uspto-grants-2009_03 |
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