Preparation of 2,5-diaminoterephthalic acid by the Hofmann degradation of pyromellitic di-imide (benzene-1,2,4,5-tetracarboxylic 1,2:4,5-di-imide) in the presence of metal salts
Nobumasa Hōjō, Hajime Yoneno
Abstract
Nobumasa Hōjō, Hajime Yoneno
Abstract
Hofmann degradation of pyromellitic di-imide gave a mixture of 4,6-diaminoisophthalic acid and 2,5-diminoterephathalic acid. Degradation of the copper of cobalt chelates of pyromellitic di-imide, or of pyromellitic di-imide in the presence of cupric or cobaltic salts, gave 2,5-diaminoterephthalic acid only. This is interpreted in terms of the structure of the chelates.
OpenAlex reports 3 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Hofmann degradation of pyromellitic di-imide gave a mixture of 4,6-diaminoisophthalic acid and 2,5-diminoterephathalic acid. Degradation of the copper of cobalt chelates of pyromellitic di-imide, or of pyromellitic di-imide in the presence of cupric or cobaltic salts, gave 2,5-diaminoterephthalic acid only. This is interpreted in terms of the structure of the chelates.
Key concepts: Imide, Pyromellitic dianhydride, Chemistry, Degradation (telecommunications), Chelation, Benzene, Cobalt, Copper