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| Other names
Potassium benzyl
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| Identifiers | |
3D model (JSmol)
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PubChem CID
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| Properties | |
| C7H7K | |
| Molar mass | 130.231 g·mol−1 |
| Appearance | Orange solid |
| Hazards | |
| Main hazards | Ignites in air |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Benzylpotassium is an organopotassium compound with the formula C6H5CH2K. It is an orange powder. Like organo-alkali metal reagents in general, benzyl potassium is highly reactive, so much so that it reacts with most solvents. It is highly air sensitive.
One early synthesis proceeds by two-step transmetallation reaction via p-tolylpotassium:[1]
A modern synthesis involves the reaction of butyllithium, potassium tert-butoxide, and toluene.[2] Although potassium hydride can also be used as a strong base for preparing potassium salts, benzyl potassium has the advantage of being molecular and hence more fast-acting.