Jump to main content
Jump to site search


Copper-catalyzed synthesis of benzo[d][1,3]dioxin-4-ones via tandem Ar-halogen bond hydroxylation and dichloromethane-based double Williamson etherification

Abstract

The reactions of o-halobenzoic acids, dichloromethane and potassium hydroxide providing benzo[d][1,3]dioxin-4-ones have been realized via the catalysis of Cu(OAc)2. Tandem Ar-X (X = I, Br) bond hydroxylation and double Williamson etherification on dichloromethane are involved during the construction of the target products.

Back to tab navigation
Please wait while Download options loads

Supplementary files

Publication details

The article was received on 15 Jan 2017, accepted on 09 May 2017 and first published on 10 May 2017


Article type: Letter
DOI: 10.1039/C7NJ00180K
Citation: New J. Chem., 2017, Accepted Manuscript
  •   Request permissions

    Copper-catalyzed synthesis of benzo[d][1,3]dioxin-4-ones via tandem Ar-halogen bond hydroxylation and dichloromethane-based double Williamson etherification

    Y. Liu, M. Huang and W. Li, New J. Chem., 2017, Accepted Manuscript , DOI: 10.1039/C7NJ00180K

Search articles by author