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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85251Generated: October 29, 2026

Ammonium Acetate → 2-[4-[2-[4-[2-(4-dibutylamino-2-methoxyphenyl)vinyl]phenyl]vinyl]-3-cyano-5,5-dimethyl-2(5H)-furanylidene]propanedinitrile

https://huagongshe.com/reaction/85251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
Reactant2-[3-Cyano-4,5,5-trimethylfuran-2(5H)-ylidene]malononitrileHCID 9990345—
Reactant4-[2-(4-Dibutylamino-2-methoxyphenyl)vinyl]benzaldehydeHCID 86667549—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product2-[4-[2-[4-[2-(4-dibutylamino-2-methoxyphenyl)vinyl]phenyl]vinyl]-3-cyano-5,5-dimethyl-2(5H)-furanylidene]propanedinitrileHCID 8666755092.6%

Reaction Steps

In 15 ml of ethanol and 5 ml of tetrahydrofuran were dissolved 500 mg (1.37 mmol) of 4-[2-(4-dibutylamino-2-methoxyphenyl)vinyl]benzaldehyde and 300 mg (1.51 mmol) of 2-(3-cyano-4,5,5-trimethyl-2(5H)-furanylidene) propanedinitrile. To this mixture was added 106 mg of ammonium acetate, and the mixture was stirred at room temperature for 23 hours. The solvent was evaporated off in a reduced pressure. The residue was washed with ethanol and then purified by silica gel column chromatography. The crystal was washed with ethanol to give 693 mg of a black powder (yield: 92.6%; mp: 258-260° C.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846955B2
Source datasetuspto-grants-2014_09
ORD IDord-1c59827ae4c646e8a7cf6cea46b42a3a
Source noteuspto-grants-2014_09