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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85269Generated: October 29, 2026

[3-Cyano-4,5-dimethyl-5-(trifluoromethyl)furan-2(5H)-ylidene]malononitrile → HCID 86667561, compound

https://huagongshe.com/reaction/85269

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[3-Cyano-4,5-dimethyl-5-(trifluoromethyl)furan-2(5H)-ylidene]malononitrileHCID 22020292—
Reactant5-[2-(8-methoxy-2,3,6,7-tetrahydro-1H,5H-benzo[ij]quinolizine-9-yl) vinyl]thiophene-2-carboaldehydeHCID 86667559—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86667561HCID 8666756178.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

In 5 ml of ethanol and 1.5 ml of tetrahydrofuran were dissolved 135 mg (0.40 mmol) of 5-[2-(8-methoxy-2,3,6,7-tetrahydro-1H,5H-benzo[ij]quinolizine-9-yl)vinyl]thiophene-2-carboaldehyde and 110 mg (0.43 mmol) of 2-(3-cyano-4,5-dimethyl-5-trifluoromethyl-2(5H)-furanylidene)propanedinitrile. The mixture was stirred with heating at 60° C. for 3.5 hours. The solvent was evaporated off and the residue was washed with ethanol. The residue was purified by silica gel column chromatography and washed with methanol to give 178 mg of a dark brown crystal (yield: 78.1%; mp: 159-161° C.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846955B2
Source datasetuspto-grants-2014_09
ORD IDord-daa8de0bd3e5429a91046efd19f75a3e
Source noteuspto-grants-2014_09