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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601653Generated: October 29, 2026

Pyridine → HCID 23158307, compound

https://huagongshe.com/reaction/601653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant7-hydroxy-2-methyl-4H-1-benzopyran-4-oneHCID 5355309—
SolventWaterHCID 962—
ProductHCID 23158307HCID 23158307—

Reaction Steps

Under nitrogen atmosphere, 0.2 ml of trifluoromethansulfonic anhydride was added at 0° C. to 3 ml solution of pyridine with 10 mg of 7-hydroxy-2-methyl-4H-chromen-4-one, and the mixture was stirred at room temperature for 2 hours. Water was added to the reaction solution, extracted with ethyl acetate. Ethyl acetate layer was washed with saturated saline solution, and dried with anhydrous sodium sulfate. The solvents were distilled outunder reduced pressure, and the residues were separated and purified by silicagel chromatography (hexane/ethyl acetate=10/1) to obtain 112 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-dbc39647c4f44499920a8e40a616d81d
Source noteuspto-grants-2011_03