Dibenzyl ketone
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| Names | |
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| IUPAC name
1,3-diphenylpropan-2-one | |
| Identifiers | |
| 3D model (JSmol) |
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| ChemSpider | |
| ECHA InfoCard | 100.002.728 |
| EC Number | 203-000-0 |
| PubChem CID |
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| Properties | |
| C15H14O | |
| Molar mass | 210.28 g·mol−1 |
| Appearance | light yellow solid |
| Density | 1.069 g/cm3 |
| Melting point | 32 to 34 °C (90 to 93 °F; 305 to 307 K) |
| Boiling point | 330 °C (626 °F; 603 K) |
| -131.7·10−6 cm3/mol | |
| Hazards | |
| Flash point | 149.4 °C (300.9 °F; 422.5 K) |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is  ?) | |
| Infobox references | |
Dibenzyl ketone, or 1,3-diphenylacetone, is an organic compound composed of two benzyl groups attached to a central carbonyl group. This results in the central carbonyl carbon atom being electrophilic and the two adjacent carbon atoms slightly nucleophilic. For this reason, dibenzyl ketone is frequently used in an aldol condensation reaction with benzil (a dicarbonyl) and base to create tetraphenylcyclopentadienone. Vera Bogdanovskaia is credited with the classification of dibenzyl ketone.
Preparation
Phenylacetone self condenses to form dibenzyl ketone.
One method is[1] where phenylacetic acid is reacted with acetic anhydride and anhydrous potassium acetate and refluxed for two hours at 140−150 °C the mixture is distilled slowly so that the distillate is mostly acetic acid, from 45 minutes into the distillation carbon dioxide is released, the distillation takes 75 minutes, carbon dioxide is still being evolved when distillation is stopped the resultant liquid is a mixture of dibenzyl ketone and minor impurities, note if this mixture is heated above 200−205 °C resinification occurs with a decrease in the yield of the ketone.
References
- ↑ J. Am. Chem. Soc., 1936, 58 (7), pp 1240–1240