Hexamethylphosphoramide, often abbreviated HMPA, is a phosphoramide (an amide of phosphoric acid) with the chemical formula This colorless liquid is used as a solvent in organic synthesis.
Structure and reactivity
HMPA is the oxide of tris(dimethylamino)phosphine, P(NMe
2)
3. Like other phosphine oxides (such as triphenylphosphine oxide), the molecule has a tetrahedral core and a P=O bond that is highly polarized, with significant negative charge residing on the oxygen atom.
Compounds containing a nitrogen–phosphorus bond typically are degraded by hydrochloric acid to form a protonated amine and phosphate.
It dissolves alkali metal salts
Applications
HMPA is a specialty
solvent for
,
gases, and organometallic compounds. It improves the selectivity of lithiation reactions by breaking up the
oligomers of
lithium bases such as
butyllithium. Because HMPA selectively solvates cations, it accelerates otherwise slow S
N2 reactions by generating more bare anions. The basic
nitrogen centers in HMPA coordinate strongly to Li
+.
HMPA is a ligand in the useful reagents based on molybdenum peroxide complexes, for example, MoO(O2)2(HMPA)(H2O) is used as an oxidant in organic synthesis.
Alternative reagents
Dimethyl sulfoxide can often be used in place of HMPA as a cosolvent. Both are strong
hydrogen bond acceptors, and their oxygen atoms bind metal
. Other alternatives to HMPA include the
N,
N′-tetraalkylureas
DMPU (dimethylpropyleneurea)
or DMI (1,3-dimethyl-2-imidazolidinone).
Tripyrrolidinophosphoric acid triamide (TPPA) has been reported to be a good substitute reagent for HMPA in reductions with samarium diiodide
and as a
Lewis base additive to many reactions involving
samarium .
Toxicity
HMPA is only mildly toxic but has been shown to cause cancer in rats.
[ HMPA can be degraded by the action of hydrochloric acid.
]
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