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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373208Generated: October 31, 2026

Acetic Acid → ethyl (2Z)-2-benzoyl-3-(5-methyl-3-pyridyl)acrylate

https://huagongshe.com/reaction/2373208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthyl benzoylacetateHCID 7170—
ReactantPiperidineHCID 8082—
Reactant5-Methylpyridine-3-carbaldehydeHCID 14141158—
SolventEthanolHCID 702—
Productethyl (2Z)-2-benzoyl-3-(5-methyl-3-pyridyl)acrylateHCID 86602398101.1%

Reaction Steps

A mixture of 5-methylnicotinaldehyde (400 mg), ethyl benzoylacetate (635 mg), AcOH (0.15 ml), piperidine (0.15 ml) in EtOH (5 ml) was stirred at room temperature for 24 hours. After evaporation, the residue was diluted with saturated aqueous NaHCO3 and extracted with EtOAc. The organic layer was washed with brine, dried over anhydrous MgSO4 and concentrated in vacuo to give ethyl (2Z)-2-benzoyl-3-(5-methyl-3-pyridyl)acrylate (986 mg) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459451B2
Source datasetuspto-grants-2008_12
ORD IDord-27d42d51e999429aac87dae60e9849ad
Source noteuspto-grants-2008_12