Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Adipic Acid | HCID 196 | — |
| Reactant | 2,4-Dinitroaniline | HCID 7321 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,2,4-Benzenetriamine | HCID 69206 | — |
Reaction Steps
91 Parts of finely ground 2,4-dinitro-aniline together with 73 parts of adipic acid, 10 parts of a commercial-type nickel catalyst and 400 parts by volume of water were charged into a hydrogenation autoclave. After the autoclave had been sealed, hydrogenation was effected in the usual manner at a temperature ranging from 60 to 100° C., while keeping the hydrogen pressure constant for about half an hour after the end of hydrogenation. For evidencing 1,2,4-triamino-benzene obtained, residual hydrogen was released, and the mixture was freed from the catalyst by filtration through a pressure filter under 20 atmsg. nitrogen and the filtrate passed into another flask flushed with nitrogen. The urea compound was prepared as described in Example 1. 62 Grams of a compound having a melting point higher than 335° C. were obtained. The following table shows accordance of the analytical data with the calculated values of the formula
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04141917 |
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| Source dataset | uspto-grants-1979_02 |
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| ORD ID | ord-40e66a64eb1a41e5a367bacded43fe19 |
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| Source note | uspto-grants-1979_02 |
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