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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732838Generated: October 25, 2026

Acetic Acid → 1,4-Bis(2-carbethoxy-2-cyano-1-methylethenyl)benzene

https://huagongshe.com/reaction/1732838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTolueneHCID 1140—
ReactantEthyl cyanoacetateHCID 7764—
Reactant1,4-DiacetylbenzeneHCID 13888—
ReactantAmmonium AcetateHCID 517165—
SolventWaterHCID 962—
Product1,4-Bis(2-carbethoxy-2-cyano-1-methylethenyl)benzeneHCID 3393270—

Reaction Steps

A mixture of p-diacetylbenzene (20.25 g, 0.125 mole), ethyl cyanoacetate (28.3 g, 0.25 mole), ammonium acetate (3.85 g) and acetic acid (10 g) was combined in a 500 ml glass round-bottom flask with toluene (150 ml) and refluxed for 12 hours. A Dean-Stark trap was employed to trap water formed during the reaction. Refluxing was discontinued and the solvent evaporated. The residue containing crude product was distilled under reduced pressure. One fraction, boiling point range 177° C.-195° C. (0.6 mm) amounting to 20.6 g was identified as predominately the 1:1 condensation product. A second fraction, boiling point ~200° C. yielded 18.2 g of 1,4-bis(2-carbethoxy-2-cyano-1-methylethenyl)benzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04239694
Source datasetuspto-grants-1980_12
ORD IDord-661de65b8eb347258833b73f9081b1fe
Source noteuspto-grants-1980_12