Lithium tetramethylpiperidide

Lithium tetramethylpiperidide

Names
IUPAC name Lithium tetramethylpiperidide
Systematic IUPAC name 1-Lithio-2,2,6,6-tetramethylpiperidine
Identifiers
CAS Number	38227-87-1 Y
3D model (JSmol)	Interactive image Interactive image Cyclic tetramer: Interactive image
ChemSpider	21428984 Y
PubChem CID	11051814
InChI InChI=1S/C9H18N.Li/c1-8(2)6-5-7-9(3,4)10-8;/h5-7H2,1-4H3;/q-1;+1 Y Key: ANYSGBYRTLOUPO-UHFFFAOYSA-N Y
SMILES [Li]N1C(C)(C)CCCC1(C)C CC1(C)CCCC(C)(C)N1[Li] Cyclic tetramer: CC1(C)CCCC(C)(C)[N+]01[Li-][N+]1(C(C)(C)CCCC1(C)C)[Li-][N+]1(C(C)(C)CCCC1(C)C)[Li-][N+]1([Li-]0)C(C)(C)CCCC1(C)C
Properties
Chemical formula	LiC9H18N
Molar mass	147.19 g·mol−1
Acidity (pKa)	37
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Y verify (what is YN ?) Infobox references

Lithium tetramethylpiperidide (often abbreviated LiTMP or LTMP) is a chemical compound with the molecular formula LiC₉H₁₈N. It is used as a non-nucleophilic base, being comparable to LiHMDS in terms of steric hindrance.

Synthesis

It is synthesised by the deprotonation of 2,2,6,6-tetramethylpiperidine with n-butyllithium at −78 °C. Recent reports show that this reaction can also be performed 0 °C. The compound is stable in a THF/ethylbenzene solvent mixture and is commercially available as such.

Structure

Like many lithium reagents it has a tendency to aggregate, forming a tetramer in the solid state.

See also

• Lithium diisopropylamide
• Lithium amide