Paper
RSC Advances
obtained was puried over a short column of silica gel to give
the product 3.
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General procedure for the synthesis of
bis(aminothiocarbonyl)disuldes
To a solution of amine (4 mmol) in 5 mL THF in a 25 mL ask
was added CS2 (4.8 mmol) followed by CAN (0.002 mmol). The
mixture was stirred for 10 min with a stopper on the ask and
then 9 h under open-air at room temperature. The solvent was
evaporated under reduced pressure to get the crude product.
Then CH2Cl2 (10 mL), HCl (1 M, 2 mL) was added and stirred for
10 min. The aqueous phase was separated and extracted with
CH2Cl2 (5 mL ꢁ 2). All the CH2Cl2 layers were combined and
dried over anhydrous MgSO4. The solution was evaporated
under reduced pressure to about 2 mL, and CH3OH (5–10 mL)
was added. The precipitate was ltered and dried under
ambient atmosphere to get the product.
Acknowledgements
We thank the National Natural Science Foundation of China
(Grant no. 20802049) for nancial supports. We are also grateful
to Ms. Jing-Jing Li for repeating the experiments.
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