HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225510Generated: October 29, 2026
α-Formyl-3-pyridineacetonitrile → HCID 23122145, compound
https://huagongshe.com/reaction/225510
Participants
| Role | Name | HCID | Charge |
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| Reactant | α-Formyl-3-pyridineacetonitrile | HCID 23336303 | — |
| Reactant | HCID 43174172 | HCID 43174172 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 23122145 | HCID 23122145 | 83% |
Reaction Steps
To an acetic acid (30 mL) solution of ethyl 3-{[(methoxycarbonyl)methyl]amino}propanate (6.720 g) was added a crude product of 3-oxo-2-(3-pyridyl)propanenitrile (7.826 g), and the mixture was stirred at 80° C. for 2 days. The reaction solution was cooled to room temperature, and the solvent was distilled off under reduced pressure. The residue was diluted with water, and sodium carbonate was added thereto for neutralization, followed by extracting the solution with ethyl acetate. The organic layer was washed with saturated brine, and dried over sodium sulfate, which was then filtered for separation. Thereafter, the solvent was distilled off under reduced pressure. The residue was purified by column chromatography on silica gel (hexane/ethyl acetate=1/3), to obtain the title compound (7.521 g, yield 83%). The ESI/MS data of the compound are given below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07557113B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-81037738e25f47dfaf52ac97195adb7e |
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| Source note | uspto-grants-2009_07 |
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