• 제목/요약/키워드: N,N,N',N'-Tetrachlorobenzene-1,3-disulfonamide (TCBDA)

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N,N,N',N'-Tetrahalobenzene-1,3-disulfonamide/PPh3 as an Efficient System for the Preparation of Alkyl Halides

  • Ghorbani-Vaghei, Ramin;Shiri, Lotfi;Ghorbani-Choghamarani, Arash
    • Bulletin of the Korean Chemical Society
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    • 제34권3호
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    • pp.820-822
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    • 2013
  • N,N,N',N'-Tetrabromobenzene-1,3-disulfonamide (TBBDA)/$PPh_3$ and N,N,N',N'-tetrachlorobenzene-1,3-disulfonamide (TCBDA)/$PPh_3$ are two highly reactive reagent systems for the conversion of alcohols corresponding into alkyl chlorides and bromides in moderate to excellent yields in dichloromethane at room temperature under mild and neutral conditions.

Poly(N,N'-Dichloro-N-ethyl-benzene-1,3-disulfonamide) and N,N,N',N'-Tetrachlorobenzene-1,3-disulfonamide as Efficient Reagents to Direct Oxidative Conversion of Thiols and Disulfide to Sulfonyl Chlorides

  • Veisi, Hojat;Ghorbani-Vaghei, Ramin;Mahmoodi, Jafar
    • Bulletin of the Korean Chemical Society
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    • 제32권10호
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    • pp.3692-3695
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    • 2011
  • Poly(N,N'-Dichloro-N-ethyl-benzene-1,3-disulfonamide) (PCBS) and N,N,N',N'-Tetrachlorobenzene-1,3-disulfonamide (TCBDA) were found to be a mild and efficient reagent for the direct oxidative conversion of sulfur compounds to the corresponding arenesulfonyl chlorides in good to excellent yields through the oxidative chlorination. The overall process is simple, practical, and it provides convenient access to a variety of aryl or heteroarylsulfonyl chlorides. The mild reaction conditions and the broad substrate scope render this method attractive, and complementary to existing syntheses of aryl or heteroarylsulfonyl chlorides.