Electrochemically generated base synthesis of thiazolidine-2-thiones was written by Medini, Hayet;Mekni, Nejib Hussein;Boujlel, Khaled. And the article was included in Journal of Sulfur Chemistry in 2015.Formula: C13H19NO This article mentions the following:
The electrolysis of secondary β-amino alcs. in the presence of carbon disulfide using an electrogenerated base (EGB) to promote the reaction of the synthesis of thiazolidine-2-thione was reported. The EGB was prepared by probase-free electrolysis of acetonitrile under galvanostatic conditions using a sacrificial magnesium anode. The reaction produced the corresponding heterocyclic thiazolidine-2-thiones in satisfactory yields. The compounds thus obtained were fully characterized by IR, 1H, 13C NMR spectroscopy, HRMS and elementary anal. In the experiment, the researchers used many compounds, for example, Trans-2-(benzylamino)cyclohexanol (cas: 40571-86-6Formula: C13H19NO).
Trans-2-(benzylamino)cyclohexanol (cas: 40571-86-6) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Formula: C13H19NO
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts