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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ethyl 2-pyridinecarboxylate | HCID 17307 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 3-oxo-3-(pyridin-2-yl)propanoate | HCID 2736461 | 91% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07511056B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-553d874a2d1b469fb510ce29b1584ada |
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| Source note | uspto-grants-2009_03 |
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