Dutta, Soumya published the artcileIodine mediated direct coupling of benzylic alcohols with dithiocarbamate anions: An easy access of S-benzyl dithiocarbamate esters under neat reaction condition, Recommanded Product: Benzyl diethylcarbamodithioate, the publication is Tetrahedron Letters (2020), 61(41), 152382, database is CAplus.
An efficient, metal and solvent free synthesis of S-benzylic dithiocarbamate esters has been demonstrated via the iodine mediated direct C-S coupling of benzylic alcs. with dithiocarbamate anions generated in-situ by the reactions of amines and carbon disulfide. All the reactions were very fast (15-30 min) and performed under open air atm. Cyclic and acyclic secondary amines, primary amine, aromatic amine actively participated in the one-pot coupling reactions with different benzylic alcs. Non benzylic alcs. offer the synthesis of O-thiocarbamate compounds under the identical reaction condition.
Tetrahedron Letters published new progress about 3052-61-7. 3052-61-7 belongs to esters-buliding-blocks, auxiliary class Amine,Benzene,Amide, name is Benzyl diethylcarbamodithioate, and the molecular formula is C12H17NS2, Recommanded Product: Benzyl diethylcarbamodithioate.
Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics