Potassium tert-butoxide
Skeletal formula of potassium tert-butoxide
Skeletal formula of potassium tert-butoxide
Ball-and-stick model of the cubane tetramer that potassium tert-butoxide adopts in
Ball-and-stick model of the cubane tetramer that potassium tert-butoxide adopts in
Names
Preferred IUPAC name
Potassium tert-butoxide
Other names
KOt-Bu, potassium t-butoxide.
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.011.583
UNII
  • InChI=1S/C4H9O.K/c1-4(2,3)5;/h1-3H3;/q-1;+1 checkY
    Key: LPNYRYFBWFDTMA-UHFFFAOYSA-N checkY
  • InChI=1/C4H9O.K/c1-4(2,3)5;/h1-3H3;/q-1;+1
    Key: LPNYRYFBWFDTMA-UHFFFAOYAU
  • [K+].[O-]C(C)(C)C
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]
GHS02: Flammable GHS05: Corrosive
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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Infobox references

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

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

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

As a base

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.

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

Potassium tert-butoxide catalyzes the reaction of hydrosilanes and heterocyclic compounds to give the silyl derivatives, with release of H2.[7]

Safety

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]

References

  1. 1 2 3 4 5 6 Caine D. (2006). "Potassiumtert-Butoxide". Potassium tert-Butoxide. e-EROS Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rp198.pub2. ISBN 0471936235.
  2. ↑ Record of Potassium tert-butoxide in the GESTIS Substance Database of the Institute for Occupational Safety and Health, accessed on 2021-12-22.
  3. ↑ William S. Johnson and William P. Schneider (1963). "β-Carbethoxy-γ,γ-diphenylvinylacetic acid". Organic Syntheses.; Collective Volume, vol. 4, p. 132
  4. ↑ 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.
  5. ↑ Brown, William; Foote, Christopher; Iverson, Brent; Anslyn, Eric (2008-01-10). Organic Chemistry. Cengage Learning. ISBN 978-0495388579.
  6. ↑ Margaret-Ann Armour (2016-04-19). Hazardous Laboratory Chemicals Disposal Guide, Third Edition. CRC Press. ISBN 9781420032383.
  7. ↑ 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)
  8. ↑ Foden, Charles R.; Weddell, Jack L. (1991-12-29). Hazardous Materials: Emergency Action Data. CRC Press. ISBN 9780873715980.
  9. ↑ Bretherick, L. (1990). Handbook of Reactive Chemical Hazards 4 ed. Dichloromethane - Reactivities / Incompatibilities in NIH National Library of Medicine. p. 475. ISBN 9781483284668.
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