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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557151Generated: October 28, 2026

Coumarin → 7-benzoyloxy-4-methyl-coumarin

https://huagongshe.com/reaction/557151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCoumarinHCID 323—
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
Reactant4-MethylumbelliferoneHCID 5280567—
SolventTetrahydrofuranHCID 8028—
Product7-benzoyloxy-4-methyl-coumarinHCID 827944—

Reaction Steps

The route shown in Scheme 1 exemplifies synthesis of the coumarin compounds of the present invention. Triethylamine is added to a solution of 7-hydroxy-4-methyl-chromen-2-one (i) and a benzoyl chloride (ii) in THF at room temperature. The reaction mixture is stirred at room temperature overnight and filtered. The filtrate is concentrated to afford a 7-benzoyloxy-4-methyl-coumarin (iii). A mixture of compound (iii) and finely powdered aluminum chloride is heated at 170° C. for 2 hours to afford an 8-benzoyl-7-hydroxy-4-methyl-chromen-2-one (iv). A mixture of compound (iv), 2-bromoacetophenone (v), and K2CO3 in CH3CN is refluxed overnight. The reaction mixture is filtered and the filtrate is concentrated. The residue is purified by column chromatography to afford a pure 8-benzoyl-4-methyl-9-phenyl-furo[2,3-h]chromen-2-one (vi).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058427B2
Source datasetuspto-grants-2011_11
ORD IDord-c1bbbc0386ab47839b4cfd0137bf8aff
Source noteuspto-grants-2011_11