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A new convenient procedure for the thionation of carbonyl compounds utilizing tetrachlorosilane–sodium sulfide

✍ Scribed by Tarek A. Salama; Abdel-Aziz S. El-Ahl; Saad S. Elmorsy; Abdel-Galil M. Khalil; Mohamed A. Ismail


Publisher
Elsevier Science
Year
2009
Tongue
French
Weight
213 KB
Volume
50
Category
Article
ISSN
0040-4039

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✦ Synopsis


A combination of tetrachlorosilane (TCS) and sodium sulfide in acetonitrile is found to be an efficient thionating reagent for aromatic aldehydes in the absence of catalysis to give the corresponding thioaldehydes as trimers in good yields. Under cobalt(II) chloride catalysis, a,b-unsaturated ketones react with TCS-Na 2 S to give the respective disulfides in good yields via the intermediacy of b-mercaptoketones at ambient temperature.


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