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The screening reactions were performed with respect to
the solvent, base, and palladium source (see Supporting
Information for the details). The oxidative addition of ArCl
to Pd(0) usually requires a bulky, electron-rich phosphine, a
secondary phosphine oxide, or an N-heterocyclic carbene
(NHC).Optimization revealed that neither phospine oxide
nor NHC ligands are effective. Electron-rich, bulky butyldi-1-adamantylphosphine
and tert -butyldicyclohexylphosphine afforded the best results, and the former was chosen because of cost considerations (Table 1). Among the bases screened,use of CsOAc, CsF, K3PO4,K2CO3, and Cs2CO3 resulted in
reasonable conversions to the product. Potassium phosphate
afforded somewhat better selectivity for monoarylation, is
cheaper than the cesium salts, and was used in all subsequent
reactions. Evaluation of palladium sources revealed that
palladium acetate is superior to all other choices. Optimiza-
tion with respect to solvent showed that the reaction proceeds
best in NMP. The optimized conditions thus include NMP
solvent, K3PO4 base, butyldi-1-adamantylphosphine ligand,and Pd(OAc)2
catalyst.

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