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...
9 KB (703 words) - 05:29, 20 May 2025
Lithium tert-butoxide is the metalorganic compound with the formula LiOC(CH3)3. A white solid, it is used as a strong base in organic synthesis. The compound...
4 KB (320 words) - 09:59, 2 April 2025
Sodium tert-butoxide forms clusters in the solid state, both hexamers and nonamers. Potassium tert-butoxide Lithium tert-butoxide Sodium tert-amyloxide...
5 KB (426 words) - 12:22, 12 February 2025
compounds. The compound was originally obtained by salt metathesis from lithium tert-butoxide and copper(I) chloride. An octameric form was obtained by alcoholysis...
2 KB (161 words) - 19:33, 12 May 2024
carbonyl compounds. tert-Butyl alcohol is deprotonated with a strong base to give the alkoxide. Particularly common is potassium tert-butoxide, which is prepared...
10 KB (727 words) - 16:30, 13 May 2025
N-Butyllithium (redirect from N-butyl lithium)
Strunk, Sven (January 1984). "The "super-basic" butyllithium/potassium tert-butoxide mixture and other lickor-reagents". Tetrahedron Letters. 25 (7): 741–744...
18 KB (1,858 words) - 17:32, 24 May 2025
Examples include sodium tert-butoxide and potassium tert-butoxide. The following diagram shows how the hindered base, lithium diisopropylamide, is used...
3 KB (354 words) - 02:44, 22 March 2024
Schlosser's base is produced by combining n-butyllithium and potassium tert-butoxide in a one-to-one ratio. The high reactivity of Schlosser's base is exploited...
3 KB (372 words) - 09:06, 12 April 2020
such as lithium diisopropylamide). The Schlosser base (or Lochmann-Schlosser base), the combination of n-butyllithium and potassium tert-butoxide, is commonly...
12 KB (1,185 words) - 19:40, 11 June 2025
ncbi.nlm.nih.gov/compound/Lithium-isopropoxide#section=Chemical-and-Physical-Properties [Li(OtBu)]6, Lithium tert-butoxide, C4H9LiO 1907-33-1 Stable to...
38 KB (600 words) - 11:12, 7 June 2025
metathesis reaction from the THF complex of molybdenum trichloride and lithium tert-butoxide: 2 MoCl3(thf)3 + 6 LiOBu-t → Mo2(OBu-t)6 + 6 LiCl + 6 thf The complex...
3 KB (209 words) - 12:10, 13 January 2025
A modern synthesis involves the reaction of butyllithium, potassium tert-butoxide, and toluene. Although potassium hydride can also be used as a strong...
2 KB (153 words) - 19:58, 12 February 2025
of propylene with Schlosser's base, a mixture of potassium tert-butoxide and butyl lithium: CH2=CHCH3 + LiC4H9 + KOC(CH3)3 → KCH2CHCH2 + C4H10 + LiOC(CH3)3...
4 KB (340 words) - 15:13, 11 June 2025
as oligomeric clusters or polymeric chains. For instance, potassium tert-butoxide consists of a cubane-like tetramer, [t-BuOK]4, that persists even in...
35 KB (3,739 words) - 07:55, 2 June 2025
transformation. Slow addition of preformed hydrazones to potassium tert-butoxide in DMSO as reaction medium instead of glycols allows hydrocarbon formation...
41 KB (4,214 words) - 14:06, 20 May 2025
P4-t-Bu (category Tert-butyl compounds)
quantitatively (96%) under mild conditions, compared to the potassium tert-butoxide/18-crown-6 system with only 75% yield. Alkylations on weakly acidic...
15 KB (1,553 words) - 02:25, 4 June 2025
occurs in presence of a strongly basic solution, such as potassium tert-butoxide in dimethyl sulfoxide: However, the yield of this method is not substantial...
4 KB (274 words) - 08:14, 28 May 2025
Alkali metal (redirect from Lithium family)
reagent is Schlosser's base, a mixture of n-butyllithium and potassium tert-butoxide. This reagent reacts with propene to form the compound allylpotassium...
225 KB (24,165 words) - 21:49, 15 June 2025
is a poor nucleophile. Bases with steric bulk, (such as in potassium tert-butoxide), are often poor nucleophiles. For example, when a 3° haloalkane is...
14 KB (1,844 words) - 07:52, 2 March 2025
acetic acid, or 4 N hydrochloric acid Allyl — Removed with potassium tert‑butoxide DABCO in methanol, palladium on activated carbon, or diverse platinum...
57 KB (6,754 words) - 18:16, 11 June 2025
the more volatile component. In this way, ethoxides can be converted to butoxides, since ethanol (b.p. 78 °C) is more volatile than butanol (b.p. 118 °C)...
10 KB (918 words) - 18:54, 17 April 2025
recycled to 17c through treatment with potassium tert-butoxide. Treatment of pure 17c with lithium tetramethylpiperidide and (±)-camphorsulfonyl oxaziridine...
16 KB (1,478 words) - 23:58, 18 February 2025
estimated pKa of this carbon acid is near 15. Potassium tert-butoxide has been used in place of butyl lithium. Sodium amide has also been used a base....
5 KB (376 words) - 16:27, 10 June 2024
Alkoxide (redirect from T-butoxide)
Al4(OiPr)12 reagent for Meerwein–Ponndorf–Verley reduction Potassium tert-butoxide, K4(OtBu)4 basic reagent in alcohol solution for organic elimination...
10 KB (1,008 words) - 21:11, 11 December 2024
t-butoxide affords 3-tert-butoxy-1,2,3-triphenylcyclopropene, which converts to 1,2,3-triphenylcyclopropenium bromide after the elimination of tert-butoxide...
6 KB (383 words) - 16:47, 18 May 2025
The enolate was formed by the reaction of ketone 47 with potassium tert-butoxide, and subsequent reaction with phenylseleninic anhydride followed by...
15 KB (1,399 words) - 13:35, 26 August 2024
rate of reaction of this heterogeneous system, via the generation of tert-butoxide or dimsyl anion. However, these catalysts have proved ineffective for...
64 KB (7,132 words) - 16:15, 23 May 2025
alkyl is Schlosser's base, a mixture of n-butyllithium and potassium tert-butoxide. This reagent reacts with toluene to form the red-orange compound benzyl...
11 KB (1,261 words) - 00:12, 27 August 2023
good leaving groups using strong bases such as sodium and potassium tert-butoxide. The subsequent addition of a nucleophile to the triple bond has low...
77 KB (7,673 words) - 01:52, 30 May 2025
gives phosphaalkynes, one example being tert-butylphosphaacetylene. Reaction with potassium tert-butoxide cleaves one P-Si bond, giving the phosphide...
5 KB (339 words) - 10:45, 1 March 2024