Reaction #2890149
Related Literature (1)
openreactiondata ↗doi:10.6084/m9.figshare.5104873.v1; patent:US04578479
Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: In Latvijas PSR Zinatnu Akad. Vestis, Khim. Ser., (2), 204-208(1965), there is described obtaining 1,2,4-triazole-3-carboxamide starting from acetyl chloride through the six reaction steps described below: ##STR3## In Czechoslovakia Pat. No. 175,118, there is disclosed a process for preparing ethyl ester of 1,2,4-triazole-3-carboxylic acid, in which ethyl ester of thioxamide acid and formylhydrazine are subjected to reaction with each other at 50° to 60° C. to obtain ethyl (2-formylhydrazino)iminoacetate, which is then heated at 160° C. to form a closed ring by dehydration. Since ethyl ester of thioxamide acid can be synthesized by subjecting ethyl ester of oxamide acid, which is available from a reaction between ethyl oxalate and ammonia, to reaction with phosphorus pentasulfide,1,2,4-triazole-3-carboxamide can be prepared from an oxalate through the five reaction steps described below. ##STR4## In this case, hydrogen sulfide is formed as a by-product and a complicated apparatus is required for deodorization thereof. through the six reaction steps
Source ID: ord-6d955919771e42f59002ed84d766a4e7