HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Hydrochloric Acid → N-phenyl-5-nitro-2-thienylamine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Thiophene, 2-nitro- | HCID 11866 | — |
| Edukt | Benzenesulfenamide, N-phenyl- | HCID 315504 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | N-phenyl-2-nitro-3-thienylamine | HCID 13039998 | 15% |
| Produkt | N-phenyl-5-nitro-2-thienylamine | HCID 19783600 | 42% |
Reaktionsschritte
2.9 g of 2-nitrothiophene and 4 g of N-phenylbenzenesulphenamide, dissolved in 10 ml of dimethylformamide, are added dropwise to a stirred solution of 6 g of potassium tert.-butylate in 60 ml of dimethylformamide, while the temperature is kept at about -20° C. The mixture is stirred for a further 15 minutes; then an excess of dilute hydrochloric acid is added to the mixture, after which it is treated in the same way as described in Example 1. The crude product is separated by column chromatography; N-phenyl-5-nitro-2-thienylamine (melting point 186° C., yield 1.8 g, 42%) and N-phenyl-2-nitro-3-thienylamine (melting point 105° C., yield 0.7 g, 15%) are obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05262539 |
| Quelldatensatz | uspto-grants-1993_11 |
| ORD ID | ord-163f67be382447bcb75b33046858f377 |
| Quellennotiz | uspto-grants-1993_11 |