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HRID 483238作成日:2026年10月25日

Hydrazinecarboxaldehyde → Ethyl (3-formyltriazan-1-ylidene)acetate

https://huagongshe.com/reaction/483238

反応式

関与物質

役割名称HCID仕込み量
反応物HydrazinecarboxaldehydeHCID 12229—
反応物ThioxamideHCID 131714592—
反応物HCID 178524907HCID 178524907—
生成物Ethyl (3-formyltriazan-1-ylidene)acetateHCID 57358554—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04578479
出典データセットuspto-grants-1986_03
ORD IDord-6d955919771e42f59002ed84d766a4e7
出典メモuspto-grants-1986_03