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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601644Generated: October 25, 2026

Pyridine → HCID 21955570, compound

https://huagongshe.com/reaction/601644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant7-Hydroxy-4-benzopyroneHCID 5409279—
SolventWaterHCID 962—
ProductHCID 21955570HCID 21955570—

Reaction Steps

Under nitrogen atmosphere, 0.24 ml of trifluoromethansulfonic anhydride was added at 0° C. to 4 ml of pyridine solution with 180 g of 7-hydroxy-4H-chromen-4-one, and the mixture was stirred at room temperature for 5 hours. Water was added to the reaction solution, extracted with chloroform. Chloroform layer was washed with saturated saline solution, and then dried with anhydrous sodium sulfate. After distilling out the solvents under reduced pressure, residues were separated and purified with preparative thin-layer chromatography (chloroform/methanol=10/1) to obtain 83 mg of the above compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902369B2
Source datasetuspto-grants-2011_03
ORD IDord-d22f9d9a8b7c45eab93dfa0270778f9d
Source noteuspto-grants-2011_03