Abstract
A domino oxidation-acyloxylation reaction of 2-arylpyridines
with aldehydes or methylarenes under the catalysis of Cu(OAc)2 has
been developed. The strategy via C-H bond functionalization
has the advantages of good functional-group tolerance, high ortho regioselectivity and no need of
any ligand or additive.
Key words
C-H activation - copper catalysis - domino
reaction - acyloxylation - oxidation
References and Notes
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General Procedure
for the Oxidation-Acyloxylation Reaction of 2-Arylpyridine
1 with Aldehydes 2
To a mixture of 2-arylpyridine
(0.25 mmol), aldehyde (0.5 mmol), Cu(OAc)2 (10 mol%,
4.5 mg), and chlorobenzene (2 mL) was added tert -butyl
hydroperoxide (2 equiv, 5.5 M in decane) dropwise at r.t. The reaction
mixture was stirred at 135 ˚C for 24 h. After the reaction,
EtOAc (10 mL) was added, and the mixture was washed with aq NaOH
(1 M, 5 mL), H2 O (10 mL), and brine (10 mL), respectively.
The filtrate was dried over Na2 SO4 and then
concentrated in vacuo. The residue was purified by column chromatography (silica
gel, PE-EtOAc as eluent) to afford the desired products 3a -n .
<A NAME="RW13211ST-9">9 </A>
Unexpectedly, when toluene was employed
under the optimal conditions, only a trace amount of benzoxylated product
was obtained.