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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951375Generated: November 3, 2026

Acetic Acid → 4-(2-Acetyl-3-oxobut-1-en-1-yl)-3-methoxybenzonitrile

https://huagongshe.com/reaction/1951375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPiperidineHCID 8082—
ReactantAcetylacetoneHCID 31261—
Reactant4-Formyl-3-methoxybenzonitrileHCID 16659251—
SolventDichloromethaneHCID 6344—
Product4-(2-Acetyl-3-oxobut-1-en-1-yl)-3-methoxybenzonitrileHCID 59186916—

Reaction Steps

21 g (130 mmol) of 4-formyl-3-methoxybenzonitrile, 14.7 ml (143 mmol) of 2,4-pentanedione, 11.2 ml (195 mmol) of acetic acid and 2.6 ml (26 mmol) of piperidine in 400 ml of dry dichloromethane are stirred under reflux with a water trap for 24 h. After cooling, the reaction solution is washed successively with saturated sodium bicarbonate solution and saturated sodium chloride solution. The organic phase is dried over magnesium sulfate and concentrated. The residue is recrystallized from diethyl ether. 23.2 g (92% of theory) of the title compound are obtained as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404709B2
Source datasetuspto-grants-2013_03
ORD IDord-7902c796ca9e4929bc8233ebfb11da6c
Source noteuspto-grants-2013_03