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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85246Generated: October 26, 2026

[3-Cyano-4,5-dimethyl-5-(trifluoromethyl)furan-2(5H)-ylidene]malononitrile → HCID 86667545, compound

https://huagongshe.com/reaction/85246

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[3-Cyano-4,5-dimethyl-5-(trifluoromethyl)furan-2(5H)-ylidene]malononitrileHCID 22020292—
Reactant5-[2-(2-Benzyloxy-4-dibutylaminophenyl)vinyl]thiophene-2-carboaldehydeHCID 86667543—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86667545HCID 8666754594%

Reaction Steps

In 10 ml of ethanol and 2 ml of tetrahydrofuran were dissolved 730 mg (1.63 mmol) of 5-[2-(2-benzyloxy-4-dibutylaminophenyl)vinyl]thiophene-2-carboaldehyde and 380 mg (1.5 mmol) of 2-(3-cyano-4,5-dimethyl-5-trifluoromethyl-2(5H)-furanylidene)propanedinitrile. The mixture was stirred at room temperature for 19 hours and further stirred with heating at 50° C. for 6 hours. The solvent was evaporated off and the residue was washed with ethanol to give 860 mg of a dark reddish brown crystal (yield: 94.0%; mp: 184-185° C.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846955B2
Source datasetuspto-grants-2014_09
ORD IDord-3be58c943823444a99fd5ce267518f27
Source noteuspto-grants-2014_09