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 language | English |
|---|---|
| Pages (from-to) | 2390-2394 |
| Number of pages | 5 |
| Journal | Organic Chemistry Frontiers |
| Volume | 5 |
| Issue number | 15 |
| DOIs | |
| State | Published - 7 Aug 2018 |
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