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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85257Generated: October 29, 2026

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

https://huagongshe.com/reaction/85257

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]-2,5-dimethylbenzaldehydeHCID 86667554—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product2-[4-[2-[4-[2-(4-dibutylamino-2-methoxyphenyl) vinyl]-2,5-dimethylphenyl]vinyl]-3-cyano-5,5-dimethyl-2(5H)-furanylidene]propanedinitrileHCID 8676280956.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

In 6 ml of ethanol and 2 ml of tetrahydrofuran were dissolved 250 mg (0.64 mmol) of 4-[2-(4-dibutylamino-2-methoxyphenyl) vinyl]-2,5-dimethylbenzaldehyde and 140 mg (0.70 mmol) of 2-(3-cyano-4,5,5-trimethyl-2(5H)-furanylidene) propanedinitrile. To this mixture was added 49 mg of ammonium acetate, and the mixture was stirred at 70° C. for 4 hours. The solvent was evaporated off, and the residue was purified by silica gel column chromatography and washed with ethanol to give 205 mg of a black powder (yield: 56.2%; mp: 242-244° C.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846955B2
Source datasetuspto-grants-2014_09
ORD IDord-50f726ccee5d403ca9460fe44ff0b34b
Source noteuspto-grants-2014_09