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letter
| Synlett 2001; 2001: 0970-0973 DOI: 10.1055/s-2001-14636 |
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Nickel-on-Charcoal-Catalyzed Reductions of Aryl Chlorides |
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| Bruce H. Lipshutz*, Takashi Tomioka, Kimihiko Sato |
| *Department of Chemistry & Biochemistry University of California, Santa Barbara, CA 93106, USA; Fax + 1 805 8 93 82 65; E-mail: lipshutz@chem.ucsb.edu |
Exposure of (functionalized) aryl chlorides to catalytic quantities of nickel-on-charcoal in the presence of stoichiometric amounts of Me2NH · BH3/K2CO3 in refluxing acetonitrile leads to high yields of reduced arenes. PCBs are also reduced under these conditions. The method is highly tolerant of moisture.
aryl chlorides - dechlorination - heterogeneous catalysis - nickel-on-charcoal
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