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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255651Generated: October 29, 2026

Acetic Anhydride → HCID 54547794, compound

https://huagongshe.com/reaction/255651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant4-PyridinecarboxaldehydeHCID 13389—
ReactantHCID 14027755HCID 14027755—
SolventWaterHCID 962—
ProductHCID 54547794HCID 5454779444.1%

Reaction Steps

To 0.7 g of 1-(4-fluorophenyl)-6-methyl-4-oxo-1,4-dihydronicotinic acid was added 0.33 g of isonicotinaldehyde and 0.61 g of acetic anhydride, and they were refluxed for 5 hours. After completion of the reaction, 30 ml of water was added to the reaction mixture, and the mixture was successively extracted with three 30-ml portions of chloroform. The chloroform layer was separated, washed with 20 ml of a saturated aqueous solution of sodium chloride, and then dried with anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure to obtain 0.42 g of 1-(4-fluorophenyl)-6-[2-(pyridin-4-yl)ethenyl]-4-oxo-1,4-dihydronicotinic acid having a melting point of 205°-215° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04698352
Source datasetuspto-grants-1987_10
ORD IDord-91e4ca6d55aa415fa706c6b223c9cbf9
Source noteuspto-grants-1987_10