HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557151Generated: October 28, 2026
Coumarin → 7-benzoyloxy-4-methyl-coumarin
https://huagongshe.com/reaction/557151
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Coumarin | HCID 323 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Methylumbelliferone | HCID 5280567 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-benzoyloxy-4-methyl-coumarin | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08058427B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-c1bbbc0386ab47839b4cfd0137bf8aff |
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| Source note | uspto-grants-2011_11 |
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