thioacetamide การใช้

• The actual rearrangement reaction takes place when the amine group attacks the thiocarbonyl in a nucleophilic addition temporarily forming an aziridine and the thioacetamide by tautomerization.
• "' Thioacetamide "'is an organosulfur compound with the S . This white crystalline solid is soluble in water and serves as a source of sulfide ions in the synthesis of organic and inorganic compounds.
• The reagent used can be any substance that gives S 2 & minus; ions in such solutions; most commonly used are hydrogen sulfide ( at 0.2-0.3 M ), thioacetamide ( at 0.3-0.6 M ).