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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2427365Erstellt: 26. Oktober 2026

4-Bromo-2-fluoroaniline → N-(4-bromo-2-fluorophenyl)-N-(6-trifluoromethoxy-1,3-benzothiazol-2-yl)amine

https://huagongshe.com/reaction/2427365

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Bromo-2-fluoroanilineHCID 123050—
Edukt2-Chloro-6-(trifluoromethoxy)-1,3-benzothiazoleHCID 10037924—
Lösungsmittel1-ButanolHCID 263—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktN-(4-bromo-2-fluorophenyl)-N-(6-trifluoromethoxy-1,3-benzothiazol-2-yl)amineHCID 2198577858,1%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

In a 250-mL round-bottom flask, 2-chloro-6-trifluoromethoxy-1,3-benzothiazole (5.36 g, 21.14 mmol) and 4-bromo-2-fluoroaniline (4.82 g, 25.36 mmol) were combined in 100 mL n-butanol containing 1% 4.0 M HCl in dioxane, and heated at 90° C. overnight. The mixture was cooled to rt and the solvent was removed under reduced pressure. Ethyl acetate (50 mL) was added, and the mixture was ultrasonicated by suspending the flask in an ultrasonication bath for 30 minutes. The mixture was filtered, and the filtrate was concentrated under reduced pressure. Acetonitrile (50 mL) was added to the mixture, which was then ultrasonicated for 30 minutes and then filtered to provide the product as a white solid (5 g, 58%). LC-MS m/z 409.1 (MH+), ret. time 4.02 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07968576B2
Quelldatensatzuspto-grants-2011_06
ORD IDord-c81b6845ca7d4afe9ff03fb885f3f261
Quellennotizuspto-grants-2011_06