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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255644Generated: October 29, 2026

5-Nitrofurfural → HCID 20183842, compound

https://huagongshe.com/reaction/255644

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-NitrofurfuralHCID 12774—
ReactantHCID 15591126HCID 15591126—
SolventEthanolHCID 702—
ProductHCID 20183842HCID 2018384231.4%

Reaction Steps

In 10 ml of ethanol were suspended 0.3 g of 6-(4-aminophenyl)-1-(4-fluorophenyl)-4-oxo-1,4-dihydronicotinic acid and 0.15 g of 5-nitrofurfural, and the suspension was subjected to reaction at 80° C. for 2 hours. After completion of the reaction, the reaction mixture was cooled to room temperature and the insolubles were removed by filtration. The solvent was removed by distillation under reduced pressure. Then, 10 ml of diethyl ether was added to the residue, and the insolubles were collected by filtration to obtain 0.13 g of 1-(4-fluorophenyl)-6-[4-{(5-nitrofurfurylidene)amino}-phenyl]-4-oxo-1,4-dihydronicotinic acid having a melting point of 129°-131° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04698352
Source datasetuspto-grants-1987_10
ORD IDord-48445063fa804a3faa8920e6d5984b15
Source noteuspto-grants-1987_10