Lithium Tert-butoxide
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Lithium Tert-butoxide
Lithium tert-butoxide
Preferred IUPAC name
Lithium tert-butoxide
  • 1907-33-1
3D model (JSmol)
ECHA InfoCard 100.016.011 Edit this at Wikidata
EC Number
  • 217-611-5
  • InChI=1S/C4H9O.Li/c1-4(2,3)5;/h1-3H3;/q-1;+1
  • [Li+].CC(C)(C)[O-]
Molar mass  g·mol-1
Appearance white solid
Density 0.918 g/cm3 (hexamer)
Main hazards strong base
GHS pictograms GHS02: FlammableGHS05: CorrosiveGHS07: Harmful
GHS Signal word Danger
H228, H251, H302, H314
P210, P235+410, P240, P241, P260, P264, P270, P280, P301+312, P301+330+331, P303+361+353, P304+340, P305+351+338, P310, P321, P330, P363, P370+378, P405, P407, P413, P420, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Lithium tert-butoxide is the metalloorganic compound with the formula LiOC(CH3)3. A white solid, it is used as a strong base in organic synthesis. The compound is often depicted as a salt, and it often behaves as such, but it is not ionized in solution. Both octameric[1] and hexameric forms have been characterized by X-ray crystallography[2]


Structure of the Li6O6C6 core of LiOBu-t hexamer, as determined by X-ray crystallography.

Lithium tert-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 sensitive and older samples are often of poor quality. It can be obtained by treating tert-butanol with butyl lithium.[3]


As a strong base, lithium tert-butoxide is easily protonated.

Lithium tert-butoxide is used to prepare other tert-butoxide compounds such as copper(I) t-butoxide and hexa(tert-butoxy)dimolybdenum(III):[4]

2 MoCl3(thf)3 + 6 LiOBu-t -> Mo2(OBu-t)6 + 6 LiCl + 6 thf

Related compounds


  1. ^ Nekola, Henning; Olbrich, Falk; Behrens, Ulrich (2002). "Kristall- und Molekülstrukturen von Lithium- und Natrium-tert-butoxid". Zeitschrift für Anorganische und Allgemeine Chemie. 628 (9-10): 2067-2070. doi:10.1002/1521-3749(200209)628:9/10<2067::AID-ZAAC2067>3.0.CO;2-N.
  2. ^ Allan, John F.; Nassar, Roger; Specht, Elizabeth; Beatty, Alicia; Calin, Nathalie; Henderson, Kenneth W. (2004). "Characterization of a Kinetically Stable, Highly Ordered, Octameric Form of Lithiumtert-Butoxide and Its Implications Regarding Aggregate Formation". Journal of the American Chemical Society. 126 (2): 484-485. doi:10.1021/ja038420m. PMID 14719943.
  3. ^ Crowther, G. P.; Kaiser, E. M.; Woodruff, R. A.; Hauser, C. R. (1971). "Esterification Of Hindered Alcohols: tert-Butyl p-Toluate". Organic Syntheses. 51: 96. doi:10.15227/orgsyn.051.0096.
  4. ^ Broderick, Erin M.; Browne, Samuel C.; Johnson, Marc J. A. (2014). Dimolybdenum and Ditungsten Hexa(Alkoxides). Inorganic Syntheses. 36. pp. 95-102. doi:10.1002/9781118744994.ch18. ISBN 9781118744994.

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