Aliphatic thioethers by s-alkylation of thiols via trialkyl borates

Deniz Gunes, Okan Sirkecioglu, Niyazi Bicak*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)

Abstract

A simple and convenient one-pot procedure is described for the synthesis of thioethers via boron esters. This procedure involves in-situ generation of alkyl sulfates by reaction of trialkyl borates with concentrated sulfuric acid and subsequent reaction with thiols in the presence of pyridine. The reactions with boron esters of primary or secondary alcohols proceed cleanly at 100C and afford aliphatic thioethers in reasonable yields (59-93%) within 24 h. Interestingly, the 1H NMR spectra of the products showed no sign of positional isomerisms. The method fails however with thiophenol and does not yield aromatic thioethers, due to electrophilic substitution at the phenyl ring.

Original languageEnglish
Pages (from-to)1685-1690
Number of pages6
JournalPhosphorus, Sulfur and Silicon and the Related Elements
Volume185
Issue number8
DOIs
Publication statusPublished - Aug 2010

Keywords

  • Alkyl sulfates
  • thioethers
  • trialkyl borates

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