Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | Aniline | HCID 6115 | — |
| Edukt | Dimethylacetamide | HCID 31374 | — |
| Edukt | 3,5-Dinitro-2,6-pyridine dimethanesulfonamide | HCID 21554886 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | 2,6-Dianilino-3,5-dinitropyridine | HCID 21554887 | 70% |
Reaktionsschritte
Under a nitrogen atmosphere, a mixture of 3,5-dinitro-2,6-pyridine dimethanesulfonamide (50 g, 0.14 mole), 200 ml aniline and 250 ml N,N-dimethylacetamide was heated with stirring to 140°C and then maintained at this temperature for 6 hours. The warm (90°C) mixture was poured onto 450 ml methanol with stirring and 20 ml triethylamine added. The precipitate was washed with methanol and dried to afford 2,6-dianilino-3,5-dinitropyridine (34.5 g, 70%) as an orange solid, mp. 224-225.5. Anal. Calcd. for C17H13N5O4 : C, 58.1; H, 3.7. Found: c, 57.4; H, 3.4.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US03943125 |
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| Quelldatensatz | uspto-grants-1976_03 |
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| ORD ID | ord-a59b774f77aa449f9522037a32e3fe9e |
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| Quellennotiz | uspto-grants-1976_03 |
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