Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactantα-Formyl-3-pyridineacetonitrileHCID 23336303—
ReactantHCID 43174172HCID 43174172—
SolventAcetic AcidHCID 176—
ProductHCID 23122145HCID 2312214583%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557113B2
Source datasetuspto-grants-2009_07
ORD IDord-81037738e25f47dfaf52ac97195adb7e
Source noteuspto-grants-2009_07