Issue 20, 2021

Visible-light-promoted photocatalyst-free alkylation and acylation of benzothiazoles

Abstract

Herein we report a protocol for the visible-light-mediated alkylation/acylation reaction of benzothiazoles. Alkyl/acyl substituted Hantzsch esters are easily prepared and rationally used as radical precursors. In the presence of BF3·Et2O and Na2S2O8, various benzothiazole derivatives were readily obtained in good yields. Our user-friendly protocol can proceed by simple irradiation with blue LEDs (λ = 465 nm) and without the assistance of external photocatalysts. The reaction is also characterized by mild conditions and scalability, thus offering an alternative and efficient tool for the synthesis of 2-functionalized benzothiazoles.

Graphical abstract: Visible-light-promoted photocatalyst-free alkylation and acylation of benzothiazoles

Supplementary files

Article information

Article type
Communication
Submitted
15 Apr 2021
Accepted
30 Apr 2021
First published
02 May 2021

Org. Biomol. Chem., 2021,19, 4487-4491

Visible-light-promoted photocatalyst-free alkylation and acylation of benzothiazoles

P. Jiang, L. Liu, J. Tan and H. Du, Org. Biomol. Chem., 2021, 19, 4487 DOI: 10.1039/D1OB00734C

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