Potassium tert-butoxide
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| Names | |||
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| Preferred IUPAC name
Potassium tert-butoxide | |||
| Other names
KOt-Bu, potassium t-butoxide.
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| Identifiers | |||
3D model (JSmol)
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| ChemSpider | |||
| ECHA InfoCard | 100.011.583 | ||
PubChem CID
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| UNII | |||
CompTox Dashboard (EPA)
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| Properties | |||
| C4H9KO | |||
| Molar mass | 112.21 g mol−1 | ||
| Appearance | solid | ||
| Melting point | 256 °C (493 °F; 529 K) | ||
| Boiling point | sublimes at 220 °C (1 mmHg) or at 140 °C (0.01 hPa) | ||
| Reacts with water | |||
| Solubility in diethyl ether | 4.34 g/100 g (25-26 °C)[1] | ||
| Solubility in Hexane | 0.27 g/100 g (25-26 °C)[1] | ||
| Solubility in Toluene | 2.27 g/100 g (25-26 °C)[1] | ||
| Solubility in THF | 25.00 g/100 g (25-26 °C)[1] | ||
| Hazards | |||
| GHS labelling:[2] | |||
 
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| Danger | |||
| H228, H252, H314 | |||
| P405 | |||
| Safety data sheet (SDS) | Oxford MSDS | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Potassium tert-butoxide (or potassium t-butoxide) is a chemical compound with the formula [(CH3)3COK]n (abbr. KOtBu). This colourless solid is a strong base (pKa of conjugate acid around 17), which is useful in organic synthesis. The compound is often depicted as a salt, and it often behaves as such, but its ionization depends on the solvent.[1]
Preparation
[edit]Potassium t-butoxide is commercially available as a solution and as a solid, but it is often generated in situ for laboratory use because samples are so moisture-sensitive and older samples are often of low purity. It is prepared by the reaction of dry tert-butyl alcohol with potassium metal.[3] The solid is obtained by evaporating these solutions followed by heating the solid. The solid can be purified by sublimation.
Structure
[edit]It crystallizes as a tetrameric cubane-type cluster. It crystallises from tetrahydrofuran/pentane at −20°C as [tBuOK·tBuOH]∞, which consists of straight chains linked by hydrogen bonding. Sublimation of [tBuOK·tBuOH]∞ affords the tetramer [tBuOK]4, which adopts a cubane-like structure. Mild Lewis basic solvents such as THF and diethyl ether do not break up the tetrameric structure, which persists in the solid, in solution and even in the gas phase.[4]
Reactions
[edit]As a base
[edit]Many modifications have been reported that influence the reactivity of this reagent. The compound adopts a complex cluster structure (the adjacent picture is a simplified cartoon), and additives that modify the cluster affect the reactivity of the reagent. For example, DMF, DMSO, hexamethylphosphoramide (HMPA), and 18-crown-6 interact with the potassium center, yielding solvent separated ion pairs such as K(DMSO)x+ and tert-BuO−. Whereas in benzene, on the other hand, the compound remains as a cluster structure, which is less basic.[1] Even in polar solvents, it is not as strong as amide bases, e.g., lithium diisopropylamide, but stronger than potassium hydroxide. Its steric bulk inhibits the group from participating in nucleophilic addition, such as in a Williamson ether synthesis or related SN2 reactions. [citation needed]
Substrates that are deprotonated by potassium t-butoxide include terminal acetylenes and active methylene compounds. It is useful in dehydrohalogenation reactions. Illustrating the latter behavior, potassium tert-butoxide reacts with chloroform yielding dichlorocarbene, which is useful for dichlorocyclopropanations.[5][6] Potassium tert-butoxide can abstract a beta-proton from alkylammonium cations, leading to the Hofmann product via an elimination reaction.
Other reactions
[edit]Potassium tert-butoxide catalyzes the reaction of hydrosilanes and heterocyclic compounds to give the silyl derivatives, with release of H2.[7]
Safety
[edit]Potassium tert-butoxide is a very strong base that rapidly attacks living tissue.
Potassium tert-butoxide forms explosive mixtures when treated with dichloromethane.[8] [9]
Related compounds
[edit]References
[edit]- ^ a b c d e f Caine D. (2006). "Potassiumtert-Butoxide". Potassium tert-Butoxide. e-EROS Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rp198.pub2. ISBN 0471936235.
- ^ Record of Potassium tert-butoxide in the GESTIS Substance Database of the Institute for Occupational Safety and Health, accessed on 2021-12-22.
- ^ William S. Johnson and William P. Schneider (1963). "β-Carbethoxy-γ,γ-diphenylvinylacetic acid". Organic Syntheses; Collected Volumes, vol. 4, p. 132.
- ^ Chisholm, Malcolm H.; Drake, Simon R.; Naiini, Ahmad A.; Streib, William E. (1991). "Synthesis and X-ray crystal structures of the one-dimensional ribbon chains [MOBut·ButOH]∞ and the cubane species [MOBut]4 (M = K and Rb)". Polyhedron. 10 (3): 337–345. doi:10.1016/S0277-5387(00)80154-0.
- ^ Brown, William; Foote, Christopher; Iverson, Brent; Anslyn, Eric (2008-01-10). Organic Chemistry. Cengage Learning. ISBN 978-0495388579.
- ^ Margaret-Ann Armour (2016-04-19). Hazardous Laboratory Chemicals Disposal Guide, Third Edition. CRC Press. ISBN 9781420032383.
- ^ Anton A. Toutov, Wen-Bo Liu, Kerry N. Betz, Alexey Fedorov, Brian Stoltz, Robert H. Grubbs (2015). "Silylation of C–H bonds in aromatic heterocycles by an Earth-abundant metal catalyst" (PDF). Nature. 518 (7537): 80–84. Bibcode:2015Natur.518...80T. doi:10.1038/nature14126. PMID 25652999. S2CID 3117834.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ Foden, Charles R.; Weddell, Jack L. (1991-12-29). Hazardous Materials: Emergency Action Data. CRC Press. ISBN 9780873715980.
- ^ Bretherick, L. (1990). Handbook of Reactive Chemical Hazards 4 ed. Dichloromethane - Reactivities / Incompatibilities in NIH National Library of Medicine. p. 475. ISBN 9781483284668.