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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133687Generated: October 26, 2026

Acetic Acid → 2-Ethylhexyl 3-(4-aminophenyl)-2-cyanoacrylate

https://huagongshe.com/reaction/133687

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDiethylamineHCID 8021—
Reactant4-AminobenzaldehydeHCID 11158—
Reactant2-Ethylhexyl cyanoacetateHCID 96359—
SolventIsopropanolHCID 3776—
Product2-Ethylhexyl 3-(4-aminophenyl)-2-cyanoacrylateHCID 5385161166.1%

Reaction Steps

36.3 g (0.3 mol) of p-aminobenzaldehyde are suspended in 450 ml of isopropanol. A mixture of 59.1 g (0.3 mol) of 2-ethylhexyl cyanoacetate and of catalyst (0.375 ml of diethylamine and 1.125 ml of acetic acid) is introduced therein. The mixture is refluxed for 5 hours. The same amount of catalyst is added again and refluxing is continued for a further 4 hours. The insoluble materials are removed by hot filtration and the mixture is concentrated to a volume of 300 ml and left to crystalize. After filtration and drying, 59.6 g (66% yield) of an orange-coloured powder are obtained, and are used without further purification for the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390916B2
Source datasetuspto-grants-2008_06
ORD IDord-241a139bf82a4c8981d30fdba0222782
Source noteuspto-grants-2008_06