Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3,3'-Diaminobenzidine | HCID 7071 | — |
| Lösungsmittel | Cyclohexanone | HCID 7967 | — |
| Produkt | HCID 18436489 | HCID 18436489 | 90% |
Reaktionsschritte
In a 200-ml flask equipped with a stirrer, a condenser and a thermometer were placed 21.4 g (100 mmol) of 3,3′-diaminobenzidine and 100 ml of cyclohexanone, followed by heating with stirring at 60° C. in a nitrogen atmosphere for 2 hours. After cooling to room temperature, cyclohexanone was removed under reduced pressure. The residue was purified by silica gel chromatography, to yield 48.1 g (90 mmol) of the target 3,3′-diaminobenzidine tetracyclohexanimine [N,N′,N″,N′″-tetracyclohexylidene-3,4,3′,4′-biphenyltetramine] in a yield of 90%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07186454B2 |
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| Quelldatensatz | uspto-grants-2007_03 |
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| ORD ID | ord-a4e875c34afd4f75a4db895afccd1b3b |
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| Quellennotiz | uspto-grants-2007_03 |
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