4.5 Article

Metal-Free Direct N-Benzylation of Sulfonamides with Benzyl Alcohols by Employing Boron Trifluoride-Diethyl Ether Complex

Journal

SYNTHESIS-STUTTGART
Volume 47, Issue 8, Pages 1101-1108

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0034-1380129

Keywords

N-benzylation; sulfonamides; benzyl alcohols; boron trifluoride-diethyl ether complex; water

Funding

  1. National Natural Science Foundation of China [21372265, 61271059]
  2. Scientific Research Fundings of the Scientific Research Foundation for the Returned Overseas Chinese Scholars, State Education Ministry
  3. Natural Science Foundation Project of CQ CSTC [cstc2013jcyjA10037]
  4. Fundamental Research Funds for the Central Universities [CDJZR14225502, CQDXWL-2013-Z012]

Ask authors/readers for more resources

N-Benzylation of sulfonamides with both primary and secondary benzyl alcohols by employing boron trifluoride-diethyl ether complex under mild reaction conditions has been developed, which is an environmentally benign and facile protocol for assembling a series of primary and secondary benzyl sulfonamides in yields up to 83%. In this coupling reaction, the beneficial role of water has been clarified in detail through control experiments.

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