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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709314Generated: October 31, 2026

Ammonium Chloride → 3-Cyano-5-[6-(N,N-di-ethenylamino)benzo[b]furanylmethylene]-4-phenyl-2-furanone

https://huagongshe.com/reaction/1709314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant6-(Diethylamino)-2-benzofurancarboxaldehydeHCID 14716710—
Reactant3-Cyano-4-phenyl-2-furanoneHCID 15165211—
SolventPyridineHCID 1049—
Product3-Cyano-5-[6-(N,N-di-ethenylamino)benzo[b]furanylmethylene]-4-phenyl-2-furanoneHCID 70361729—

Reaction Conditions

Temperature80 °C

Reaction Steps

To 5 mL of pyridine in a 15 mL round bottom flask was added 217 mg (1 mmol) of the compound of Example 2 and 172 mg (1 mmol) of 3-cyano-4-phenyl-2-furanone. The solution was heated at 80° C. for one hour, cooled and poured into 20 mL dilute NH4Cl. The resulting mixture was extracted 2X with 20 mL 3:2 hexanes Et2O and the combined organic extracts were washed once with 10 mL of water, The organic phase was dried (MgSO4) and the solvent removed by rotary evaporation. The resulting solid was purified by flash chromatography (7:2 cyclohexane/EtOA; SiO2, 1×12") to yield 292 mg of dye. Anal. calcd. for C24H20N2O3 : C, 74.2; H, 5.4; N, 7.5. Found: C, 74.0; H, 5.2; N, 6.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04948895
Source datasetuspto-grants-1990_08
ORD IDord-f6214208cbcb43348150f73e30c23ed8
Source noteuspto-grants-1990_08