Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | HCID 11222615 | HCID 11222615 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 18669516 | HCID 18669516 | 48.4% |
Reaction Steps
To a solution of 3-(2,4-difluorophenyl)-2-(4-methanesulfonylphenyl)-6-methylpyran-4-one (1.7 g; 4.5 mmoles) (compound 13) in dioxane (45 ml), selenium dioxide (2.2 g, 20 mmoles) was added and the mixture heated in a pressure vessel at 180° C. for 1 hour. After cooling, the reaction mixture was filtered, the solvent removed under reduced pressure and the residual oil purified by column chromatography with silica gel and ethyl acetate as eluent. 5-(2,4difluorophenyl)-6-(4-methanesulfonylphenyl)-4-oxo-4H-pyran-2-carbaldehyde (0.85 g) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06518303B2 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-5447d7dd997443be8bf27764f3206796 |
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| Source note | uspto-grants-2003_02 |
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