React an alcohol with Na/K hydroxide and carbon disulfide to form an alkyl xanthate salt. Then, oxidize it (electrochemically or otherwise) to form an
alkyl xanthic disulfide.
Thioanhydrides are more complicated, and require either desulfurization of the disulfide with cyanide or reaction of the alkyl xanthate salt with a
chloroformate.
Note: While tertiary xanthic disulfides/thioanhydrides are possible to make, they decompose easily. Primary and secondary alkyl groups are best.
For more information, https://www.sciencemadness.org/whisper/viewthread.php?tid=28...
Still, now I know that the OP wants to make soap, these compounds are not ideal for that purpose: they melt in hot water. |