Reaction of carbon disulfide with azide ion


Autoria(s): Lieber, Eugene; Oftedahl, Edwin; Rao, CNR
Data(s)

1963

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