2015Advanced Synthesis & CatalysisRequires access

Room‐Temperature Copper‐Catalyzed Arylation of Dimethylamine and Methylamine in Neat Water

Deping Wang, Dai‐Zhi Kuang, Fu-Xing Zhang, Chunlin Yang, Xiaoming Zhu

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Abstract

Abstract The first room‐temperature copper‐catalyzed arylations of dimethylamine and methylamine in neat water have been developed. Using a combination of CuI and 6,7‐dihydroquinolin‐8(5 H)‐one oxime as catalyst, dimethylamine is arylated with various aryl halides to give the corresponding products in good to excellent yields. Further, this catalysis enables the selective arylation of methylamine to afford the high yields of monoarylated methylamines as the sole products. magnified image

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Abstract The first room‐temperature copper‐catalyzed arylations of dimethylamine and methylamine in neat water have been developed. Using a combination of CuI and 6,7‐dihydroquinolin‐8(5 H)‐one oxime as catalyst, dimethylamine is arylated with various aryl halides to give the corresponding products in good to excellent yields. Further, this catalysis enables the selective arylation of methylamine to afford the high yields of monoarylated methylamines as the sole products. magnified image

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Available abstract

Abstract The first room‐temperature copper‐catalyzed arylations of dimethylamine and methylamine in neat water have been developed. Using a combination of CuI and 6,7‐dihydroquinolin‐8(5 H)‐one oxime as catalyst, dimethylamine is arylated with various aryl halides to give the corresponding products in good to excellent yields. Further, this catalysis enables the selective arylation of methylamine to afford the high yields of monoarylated methylamines as the sole products. magnified image

Key concepts: Dimethylamine, Methylamine, Methylamines, Chemistry, Catalysis, Halide, Aryl, Copper

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