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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85319Generated: October 30, 2026

2-[3-Cyano-4,5,5-trimethylfuran-2(5H)-ylidene]malononitrile → 2-[4-[2-[2-(tert-butyldiphenylsiloxy)-4-dibutylaminophenyl]vinyl]-3-cyano-5,5-dimethyl-2(5H)-furanylidene]propanedinitrile

https://huagongshe.com/reaction/85319

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[3-Cyano-4,5,5-trimethylfuran-2(5H)-ylidene]malononitrileHCID 9990345—
Reactant2-(Tert-butyldiphenylsiloxy)-4-dibutylaminobenzaldehydeHCID 86667603—
SolventEthanolHCID 702—
Product2-[4-[2-[2-(tert-butyldiphenylsiloxy)-4-dibutylaminophenyl]vinyl]-3-cyano-5,5-dimethyl-2(5H)-furanylidene]propanedinitrileHCID 8666760272.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

In 5 ml of ethanol were dissolved 200 mg (0.41 mmol) of 2-(tert-butyldiphenylsiloxy)-4-dibutylaminobenzaldehyde and mg (0.45 mmol) of 2-(3-cyano-4,5,5-trimethyl-2(5H)-furanylidene)propanedinitrile. After the mixture was stirred with heating at 60° C. for 3 hours, the precipitate was separated by filtration and washed with methanol. The crystal was purified by silica gel column chromatography and washed with methanol to give 199 mg of a dark brown crystal having a mp of 220-221° C. (yield: 72.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846955B2
Source datasetuspto-grants-2014_09
ORD IDord-e6a3d15e954d45108a54c8791bff0078
Source noteuspto-grants-2014_09