Synthesis of Dithioester Derivatives by Base-Mediated Fragmentation of 1,3-Dithiolanes

Hasan Pelit, Mehmet Aytug Sinmaz, Oyku Acelya Ildem, Zeynep Mert, Yigit Efe Turhan, Elif Aydin, Senem Dila Yilmaz, Andrea Mentese, Baris Yucel*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Dithioesters are important agents for chain transfer in polymer chemistry and precursors in the synthesis of heterocycles. Straightforward approaches to their synthesis are therefore in demand. Outlined herein is a method to access such compounds in one-pot. 2-Aryl-1,3-dithiolanes undergo ring fragmentation with LiHMDS in CPME to generate aryl-dithiocarboxylates in 5 min at 100 °C. These anions are subsequently captured in the second step by addition of various alkyl halides and diaryliodonium salts to furnish a large library of dithioesters in good yields. The method can be also employed in a one-pot, one-step manner for alkyl bromides and allows the synthesis of dithioesters in gram scale.

Original languageEnglish
JournalOrganic Letters
DOIs
Publication statusAccepted/In press - 2025

Bibliographical note

Publisher Copyright:
© 2025 The Authors. Published by American Chemical Society.

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