HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-Aminothiophenol → 5-(2H-1,4-benzothiazin-3-yl)-3-nitropyrocatechol
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-Aminothiophenol | HCID 8713 | — |
| Edukt | 2-Bromo-1-(3,4-dihydroxy-5-nitro-phenyl)-ethanone | HCID 21845596 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 5-(2H-1,4-benzothiazin-3-yl)-3-nitropyrocatechol | HCID 135665321 | — |
Reaktionsschritte
A mixture of 2.78 g of 2-bromo-3',4'-dihydroxy-5'-nitroacetophenone, 1.51 g of 2-aminothiophenol and 50 ml of ethanol is heated to boiling under reflux for 1 hour. The reaction mixture is then cooled to room temperature, whereupon the crystals are removed by filtration under suction. There is obtained 5-(2H-1,4-benzothiazin-3-yl)-3-nitropyrocatechol of m.p. 302'-304° (from N,N-dimethylformamide/methanol).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05389653 |
| Quelldatensatz | uspto-grants-1995_02 |
| ORD ID | ord-02a3eab13ea74001bf3f545a1f30be11 |
| Quellennotiz | uspto-grants-1995_02 |