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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951384Generated: November 2, 2026

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

https://huagongshe.com/reaction/1951384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPiperidineHCID 8082—
ReactantAcetylacetoneHCID 31261—
Reactant3-Ethyl-4-formylbenzonitrileHCID 17819327—
SolventDichloromethaneHCID 6344—
Product4-(2-Acetyl-3-oxobut-1-en-1-yl)-3-ethylbenzonitrileHCID 59603013—

Reaction Steps

885 mg (5.55 mmol) of 3-ethyl-4-formylbenzonitrile, 0.62 ml (6.11 mmol) of 2,4-pentanedione, 0.47 ml (8.33 mmol) of acetic acid and 0.11 ml (1.11 mmol) of piperidine in 40 ml of anhydrous 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 (1.07 g) is reacted further without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404709B2
Source datasetuspto-grants-2013_03
ORD IDord-c4b2be65e5b043e8b5b9f6fc349844ea
Source noteuspto-grants-2013_03