Abstract
CeCl3 catalyzes the addition of Et2 Zn to
a variety of alipahtic and aromatic aldehydes and ketones in THF
in the presence of TMSCl as a scavenger. Optimization of the applied
solvent allowed to avoid the TMSCl mediated addition using CeCl3 ·(THF)2 or
Ce(i -PrO)3 as catalysts. This
represents the first application of lanthanide compounds for the
addition of Et2 Zn to carbonyl compounds.
Key words
lanthanides - cerium - catalysis - diethylzinc - addition to carbonyls
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General Experimental
Procedure: The reactions were carried out under argon atmosphere
using Schlenk techniques. Substances, which are sensitive against
moisture and oxidation were stored in a glove box. Reactions were typically
performed on a 1.5 mmol scale. In a Schlenk tube 5 mL of solvent
were added to the catalyst (usually 0.075 mmol, 0.05 equiv).
Then, 3 mL of an 1 M solution of diethylzinc (3 mmol, 2 equiv) in
the applied solvent were transferred to the reaction via canulla.
To the reaction mixture 1.5 mL of a 1 M solution of aldehyde (1.5
mmol, 1 equiv) in the used solvent were then added slowly
by using a syringe pump. When TMSCl was used as a scavenger 1.5
mL of a 1.5 M solution (2.25 mmol, 1.5 equiv) in the chosen solvent
were added simultaneously using the same syringe pump. After careful
addition of 25 mL of sat. aq NH4 Cl or 2 N HCl, respectively,
the aqueous phase was extracted with ethylether (3 × 30
mL). The combined and dried (MgSO4 ) organic layers were
then liberated from the solvent and purified by flash chromatography
eluting with EtOAc/petroleum ether.