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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357194Generated: November 3, 2026

Pyridine → HCID 15462825, compound

https://huagongshe.com/reaction/1357194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzoyl chlorideHCID 7412—
ReactantPotassium bisulfateHCID 516920—
ReactantHCID 54712960HCID 54712960—
SolventDichloromethaneHCID 6344—
ProductHCID 15462825HCID 15462825—

Reaction Steps

Pyridine (64 μl) and benzoyl chloride (45 μl) were added to a suspension of 6-(benzofuran-2-yl)-3,5-dimethyl-4-hydroxy-2H-pyran-2-one (40 mg) in CH2Cl2 (5 ml), and the mixture was stirred at room temperature for 50 minutes. The reaction solution was poured into a KHSO4 aqueous solution and extracted with AcOEt, and the organic layer was rinsed with saturated saline and dried with MgSO4, and then filtered and concentrated. The residue was purified by silica gel column chromatography (n-hexane/AcOEt=5/1→4/1) to obtain 6-(benzofuran-2-yl)-4-benzoyloxy-3,5-dimethyl-2H-pyran-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06589984B1
Source datasetuspto-grants-2003_07
ORD IDord-d59aadcce2b848bdad78acede6fa6d89
Source noteuspto-grants-2003_07