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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 274472Erstellt: 24. Oktober 2026

2-Aminothiophenol → 5-(2H-1,4-benzothiazin-3-yl)-3-nitropyrocatechol

https://huagongshe.com/de/reaction/274472

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-AminothiophenolHCID 8713—
Edukt2-Bromo-1-(3,4-dihydroxy-5-nitro-phenyl)-ethanoneHCID 21845596—
LösungsmittelEthanolHCID 702—
Produkt5-(2H-1,4-benzothiazin-3-yl)-3-nitropyrocatecholHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05389653
Quelldatensatzuspto-grants-1995_02
ORD IDord-02a3eab13ea74001bf3f545a1f30be11
Quellennotizuspto-grants-1995_02