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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 131815Erstellt: 24. Oktober 2026

2-Aminothiazole → 2-(2,3,4-Trichlorophenoxy)-1-nitrobenzene

https://huagongshe.com/de/reaction/131815

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-AminothiazoleHCID 2155—
Edukt2,3,4-TrichlorophenolHCID 27582—
Edukt1-Fluoro-2-nitrobenzeneHCID 73895—
Edukt2-(2,3,4-Trichlorophenoxy)anilineHCID 66998815—
ProduktN-[2-(2,3,4-Trichlorophenoxy)phenyl]-N'-(thiazol-2-yl)ureaHCID 5973292955%
Produkt2-(2,3,4-Trichlorophenoxy)-1-nitrobenzeneHCID 6699911465%

Reaktionsschritte

2-(2,3,4-Trichlorophenoxy)-1-nitrobenzene (1.04 g, 65%) was prepared from 2,3,4-trichlorophenol (0.98 g, 5.0 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(2,3,4-trichlorophenoxy)aniline (0.42 g, 60%, 2.5 mmol scale) following general procedure B. N-[2-(2,3,4-Trichlorophenoxy)phenyl]-N′-(thiazol-2-yl)urea (343 mg, 55%) was prepared from 2-(2,3,4-trichlorophenoxy)aniline (420 mg, 1.5 mmol) and 2-aminothiazole (150 mg, 1.5 mmol) following the general procedure D

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07384967B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-e09b32618449401d835c3c1418665e94
Quellennotizuspto-grants-2008_06