5-Hydroxy-2(5H)-furanone
| Names | |
|---|---|
| Preferred IUPAC name
5-Hydroxyfuran-2(5H)-one | |
| Other names
5-Hydroxy-5H-furan-2-one, 2-Hydroxyfuranone-(5), β-oxo-γ-butyrolactone, 4-Oxobut-2-enoic acid, 2,5-dihydrofuran-2-one, beta-Formylacrylic acid lactol, 2-Oxo-5-hydroxy-2,5-dihydrofuran, 2-Hydroxy-2,5-dihydro-5-furanone, 5-Hydroxy-2,5-dihydrofuran-2-one; γ-Hydroxybutenolide
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| Identifiers | |
3D model (JSmol)
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| ChemSpider | |
| ECHA InfoCard | 100.112.891 |
PubChem CID
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CompTox Dashboard (EPA)
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| Properties | |
| C4H4O3 | |
| Molar mass | 100.073 g·mol−1 |
| Density | 1.503 g/mL |
| Melting point | 55 °C |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
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5-Hydroxy-2(5H)-furanone is a furanone derived from oxidation of furfural using singlet oxygen. This oxidation is carried out generally in methanol or ethanol with a sensitizer like methylene blue or Rose bengal. The mechanism of this reaction is depicted as below.