Toluene solutions of alkylmagnesium chlorides partially solvated by di
ethyl ether were investigated. Primary and secondary alkyl chlorides c
an be converted into Grignard reagents in good yields in the presence
of small amounts of ether (less than one mole per mole of halide). Ter
tiary chlorides form only monosolvated organomagnesium compounds. Ultr
asound accelerates the process. The reagents obtained are heterogeneou
s, but the solubilities of the partially solvated complexes in toluene
are fairly high. Some of the reagents disproportionate to magnesium c
hloride and the dialkylmagnesium. The extent of disproportionation dec
reases with an increase in the concentration of the reagent or in the
steric requirements of the alkyl moiety.