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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951394Generated: November 2, 2026

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

https://huagongshe.com/reaction/1951394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPiperidineHCID 8082—
ReactantAcetylacetoneHCID 31261—
Reactant3-Chloro-4-formylbenzonitrileHCID 12290550—
SolventDichloromethaneHCID 6344—
SolventCyclohexane ethylacetateHCID 21867204—
Product4-(2-Acetyl-3-oxobut-1-en-1-yl)-3-chlorobenzonitrileHCID 6741684089.8%

Reaction Steps

300 mg (1.812 mmol) of 3-chloro-4-formylbenzonitrile, 181.4 mg (1.812 mmol) of 2,4-pentanedione, 163.2 mg (2.72 mmol) of acetic acid and 30.9 mg (0.36 mmol) of piperidine are dissolved in 15 ml of dichloromethane and heated under reflux with an inverse water trap overnight. The mixture shows complete conversion (TLC check, mobile phase: cyclohexane/ethyl acetate 5:1). The mixture is diluted with dichloromethane, washed with water and saturated sodium chloride solution and dried with sodium sulfate. The solvent is removed in a rotary evaporator. 403 mg (89.8% of theory) of 4-(2-acetyl-3-oxobut-1-en-1-yl)-3-chlorobenzonitrile are obtained and are reacted without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404709B2
Source datasetuspto-grants-2013_03
ORD IDord-8344fbcb2ebf436692eb2bcd4f9543bb
Source noteuspto-grants-2013_03