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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32488Generated: October 27, 2026

Acetic Acid → 2-[1-(4-Nitrophenyl)ethylidene]malononitrile

https://huagongshe.com/reaction/32488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactantp-NitroacetophenoneHCID 7487—
ReactantMalononitrileHCID 8010—
ReactantAmmonium AcetateHCID 517165—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
SolventSodium chloride; waterHCID 57417360—
Product2-[1-(4-Nitrophenyl)ethylidene]malononitrileHCID 11042086—

Reaction Steps

p-Nitro-acetophenone (165 g/mole; 4.0 g; 24 mmoles), ammonium acetate (0.50 g) and glacial acetic acid (0.80 mL) were added to a round-bottom flask containing 20 mL toluene, and heated to reflux using a Dean-Stark trap and a reflux condenser. Separately, malononitrile (66 g/mole; 2.0 g; 30.3 mmoles) was dissolved in 5 mL dioxane and 20 mL toluene, transferred to an addition funnel and added dropwise to the heated solution of ketone. Upon completion of the addition, the system was heated for 2 hours and then cooled to room temperature. The reaction mixture was poured into 150 mL brine and 100 mL ethyl acetate. The aqueous layer was separated and washed with 50 mL ethyl acetate. The organic layers were combined and dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the crude product 2-[1-(4-nitrophenyl)-ethylidene]-malononitrile (213 g/mole) was used as such in Intermediate Example 11.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07427623B2
Source datasetuspto-grants-2008_09
ORD IDord-2d3178a7af6744be8777365630066edd
Source noteuspto-grants-2008_09