Reaction of carbon disulfide with azide ion
Data(s) |
1963
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Resumo |
Carbon disulfide reacts with azide ion to form the 1,2,3,4-thiatriazolinethionate ion and not the acyclic azido dithiocarbonate ion as previously reported. A series of salts of thiatriazoline have been prepared and none shows evidence for the presence of the azido group. Esters of thiatriazolinethione prepared by the reaction of the sodium salt with alkyl or acyl halides have been found to be either 5-(substituted) mercapto-1,2,3,4-thiatriazoles or 4-substituted 1,2,3,4-thiatriazoline-5-thiones. These structures have been assigned on the basis of degradative and spectroscopic evidence. The chemistry of the so-called azidodithiocarbonates has been reinterpreted in terms of the thiatriazole structure. |
Formato |
application/pdf |
Identificador |
http://eprints.iisc.ernet.in/28104/1/Car.pdf Lieber, Eugene and Oftedahl, Edwin and Rao, CNR (1963) Reaction of carbon disulfide with azide ion. In: Journal of Organic Chemistry, 28 (1). pp. 194-199. |
Publicador |
American Chemical Society |
Relação |
http://pubs.acs.org/doi/abs/10.1021/jo01036a046 http://eprints.iisc.ernet.in/28104/ |
Palavras-Chave | #Others |
Tipo |
Journal Article PeerReviewed |