Green carbon disulfide surrogate: Via a combination of potassium sulfide and chloroform for benzothiazine-thione and benzothiazole-thione construction

  • Wei Tan
  • , Cuihong Wang*
  • , Xuefeng Jiang
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

50 Scopus citations

Abstract

An efficient and green carbon disulfide surrogate via facile combination of potassium sulfide and chloroform has been developed. A variety of benzothiazine-thiones and benzothiazole-thiones were straightforwardly established along with the formation of five new chemical bonds in one pot from readily available starting materials, in which the widely used 2-mercaptobenzothiazole (MBT) was synthesized through this method in gram scale. Dichlorocarbene was demonstrated to be a carbon source intermediate from chloroform on the basis of control experimental studies. Meanwhile, potassium sulfide, as a trisulfur radical anion (S3 -) source, was confirmed through UV-visible spectroscopy and an EPR study.

Original languageEnglish
Pages (from-to)2390-2394
Number of pages5
JournalOrganic Chemistry Frontiers
Volume5
Issue number15
DOIs
StatePublished - 7 Aug 2018

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