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Rapid synthesis of 2,5-disubtituted 1,3,4-thiadiazoles under microwave irradiation

✍ Scribed by Mounim Lebrini; Fouad Bentiss; Michel Lagrenée


Publisher
Journal of Heterocyclic Chemistry
Year
2005
Tongue
English
Weight
60 KB
Volume
42
Category
Article
ISSN
0022-152X

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✦ Synopsis


Abstract

The one pot, three‐components condensation of aromatic aldehydes, hydrazine and sulfur in ethanol under microwave irradiation provided symmetrically 3,5‐disubstituted 1,3,4‐thiadiazoles in high yields and good purity. This reaction must be conducted under pressure of hydrogen sulfide produced in‐situ. The structure of the compounds was confirmed by ^1^H, ^13^C NMR, MS and elemental analysis.


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