Tetrapropylammonium perruthenate
 | |
| Names | |
|---|---|
| IUPAC name
Tetrapropylammonium perruthenate | |
| Identifiers | |
114615-82-6  | |
| Abbreviations | TPAP TPAPR |
| ChemSpider | 21170134  |
| Jmol interactive 3D | Image |
| |
| |
| Properties | |
| C12H28NRuO4 | |
| Molar mass | 351.43 g/mol |
| Appearance | Green solid |
| Melting point | 160 °C (320 °F; 433 K) (decomposition) |
| 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 | |
Tetrapropylammonium perruthenate (TPAP or TPAPR) is the chemical compound described by the formula N(C3H7)4RuO4. Sometimes known as the Ley–Griffith reagent, this ruthenium compound is used as a reagent in organic synthesis. This salt consists of the tetrapropylammonium cation and the perruthenate, RuO4− anion. Ruthenium tetroxide is a highly aggressive oxidant, but its one-electron reduced derivative is a mild oxidizing agent for the conversion of alcohols to aldehydes.[1] This oxidizing agent can also be used to oxidize primary alcohols all the way to the carboxylic acid. Use of a higher catalyst loading, larger amount of the co-oxidant, and addition of two equivalents of water. In this situation, the aldehyde reacts with water to form the geminal-diol hydrate, which is then oxidized again.[2]
The oxidation generates water that can be removed by adding molecular sieves. TPAP is expensive, but it can be used in catalytic amounts. The catalytic cycle is maintained by adding a stoichiometric amount of a co-oxidant such as N-methylmorpholine N-oxide or molecular oxygen.[3]
References
- ↑ Ley, Steven V.; Norman, Joanne; Griffith, William P.; Marsden (1994). "Tetrapropylammonium Perruthenate, Pr4N+RuO4−, TPAP: A Catalytic Oxidant for Organic Synthesis". Synthesis: 639–666. doi:10.1055/s-1994-25538.
|first4=missing|last4=in Authors list (help) (review article) - ↑ Xu, Z.; Johannes, C. W.; Houri, A. F.; La, D. S.; Cogan, D. A.; Hofilena, G. E.; Hoveyda, A. H. (1997). "Applications of Zr-Catalyzed Carbomagnesation and Mo-Catalyzed Macrocyclic Ring Closing Metathesis in Asymmetric Synthesis. Enantioselective Total Synthesis of Sch 38516 (Fluvirucin B1)". J. Am. Chem. Soc. 119: 10302–10316. doi:10.1021/ja972191k.
- ↑ Lenz, Roman; Ley., Steven V. (1997). "Tetra-n-propylammonium perruthenate (TPAP)-catalysed oxidations of alcohols using molecular oxygen as a co-oxidant". J. Chem. Soc., Perkin Trans. 1: 3291–. doi:10.1039/C39870001625.
- ↑ Hadfield, John A.; McGown, Alan T.; Butler, John (2000). "A High-Yielding Synthesis of the Naturally Occurring Antitumour Agent Irisquinone" (PDF). Molecules 5: 82–88. doi:10.3390/50100082.
| ||||||||||||||||||||||||||||||||||||||