HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011965Generated: October 31, 2026
Pyridine → 3-Cyclopropyl-3-oxo-2-(pyridine-4-carbonyl)-propionic acid ethyl ester
https://huagongshe.com/reaction/1011965
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ethyl 3-cyclopropyl-3-oxopropanoate | HCID 262979 | — |
| Reactant | Magnesium Chloride | HCID 5360315 | — |
| Reactant | Isonicotinoyl chloride hydrochloride | HCID 12262826 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Cyclopropyl-3-oxo-2-(pyridine-4-carbonyl)-propionic acid ethyl ester | HCID 67313757 | 79.7% |
Reaction Steps
7.5 g (48 mmol) of 3-cyclopropyl-3-oxo-propionic acid ethyl ester were dissolved in 250 ml of CH2Cl2, the solution was cooled at 0° C. and successively were added 4.71 g (49.5 mmol) of anhydrous magnesium chloride, 8.1 ml (100 mmol) of pyridine and 12.8 g (72 mmol) of isonicotinoyl chloride.hydrochloride. The yellow suspension was stirred 1 h under ice cooling and 18 h at room temperature. The reaction mixture was poured into crashed ice and extracted twice with CH2Cl2. The organic phases were washed with brine, dried over magnesium sulfate, and evaporated. The residual product was purified by column chromatography (n-heptane:EtOAc 1:1) to afford the title compound as light yellow oil (10 g, 79%). MS: 262.1 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977358B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-652dd05cae4a41e49ce76b74e89d6704 |
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| Source note | uspto-grants-2011_07 |
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