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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 71020Erstellt: 24. Oktober 2026

Ethanol → (Imidazo[2,1-b]benzothiazol-2-yl)aniline

https://huagongshe.com/de/reaction/71020

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktWaterHCID 962—
EduktSulfuric AcidHCID 1118—
EduktBenzo(d)thiazol-2-amineHCID 8706—
Edukt2-Bromo-4'-nitroacetophenoneHCID 66840—
KatalysatorIronHCID 23925—
Produkt(Imidazo[2,1-b]benzothiazol-2-yl)anilineHCID 66592992—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A mixture of 2-aminobenzothiazole (4.00 g, 26.6 mmol) and 2-bromo-4′-nitroacetophenone (7.32 g, 30.0 mmol) was refluxed in ethanol for 90 min and then the mixture was cooled to 0° C. The solid (about 2 g) was collected by filtration, washed with the minimum quantity of cold ethanol and then dissolved again in 150 ml of ethanol and added of iron powder (7.47 g, 133.75 mmol), water (30 ml) and H2SO4 12N (750 μl). The mixture was stirred at 90° C. for 1 h, then filtered on celite and washed with hot ethanol. The solvent was removed under reduced pressure and the crude material was treated with aqueous NaHCO3 (10%, 400 ml) and extracted with CH2Cl2 (3×150 ml). The organic phase was dried with anhydrous Na2SO4 and the solvent removed under reduced pressure to afford 4-[(imidazo[2,1-b]benzothiazol-2-yl)aniline.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822698B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-5cb9c0d62efe480bb4d5d681b4e59ec7
Quellennotizuspto-grants-2014_09