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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85342Generated: October 29, 2026

Ammonium Acetate → 2-[4-[2-[5-[2-(4-dibutylaminophenyl)vinyl]thiophene-2-yl]vinyl]-3-cyano-5,5-dimethyl-2(5H)-furanylidene]propanedinitrile

https://huagongshe.com/reaction/85342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
Reactant2-[3-Cyano-4,5,5-trimethylfuran-2(5H)-ylidene]malononitrileHCID 9990345—
Reactant5-[2-[4-(Dibutylamino)phenyl]vinyl]thiophene-2-carboaldehydeHCID 76563675—
SolventTetrahydrofuran ethanolHCID 21873804—
Product2-[4-[2-[5-[2-(4-dibutylaminophenyl)vinyl]thiophene-2-yl]vinyl]-3-cyano-5,5-dimethyl-2(5H)-furanylidene]propanedinitrileHCID 8666761776.1%

Reaction Steps

In an ethanol/tetrahydrofuran mixed solvent were dissolved 170 mg (0.50 mmol) of 5-[2-[4-(dibutylamino)phenyl]vinyl]thiophene-2-carboaldehyde and 110 mg (0.55 mmol) of 2-(3-cyano-4,5,5-trimethyl-2(5H)-furanylidene) propanedinitrile. To this mixture, 42 mg of ammonium acetate was added, and the mixture was stirred at room temperature. The solvent was evaporated off. The residue was purified by silica gel column chromatography and washed with ethanol to give 198 mg of a black crystal having amp of 208-209° C. (yield: 76.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846955B2
Source datasetuspto-grants-2014_09
ORD IDord-c4ca73226f7b40f984d1dc3b0f4872f9
Source noteuspto-grants-2014_09