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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 78358Erstellt: 23. Oktober 2026

2-Methoxy-5-(trifluoromethyl)aniline → 3-(4-Aminophenoxy)benzoic acid

https://huagongshe.com/de/reaction/78358

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Methoxy-5-(trifluoromethyl)anilineHCID 600637—
EduktBenzene, 2-isocyanato-1-methoxy-4-(trifluoromethyl)-HCID 11983909—
Edukt3-(4-Aminophenoxy)benzoic acidHCID 23009036—
Produkt3-(4-Aminophenoxy)benzoic acidHCID 23009036—
ProduktN-(5-(trifluoromethyl)-2-methoxyphenyl)-N'-(3-carboxyphenyl)ureaHCID 23614600—

Reaktionsschritte

Entry 39: 4-(3-Carboxyphenoxy)aniline was synthesized according to Method A11. 5-(Trifluoromethyl)-2-methoxyaniline was converted into 5-(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method B1. 4-(3-Carboxyphenoxy)aniline was reacted with 5-(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method C1f to afford N-(5-(trifluoromethyl)-2-methoxyphenyl)-N′-(3-carboxyphenyl)urea, which was coupled with 4-morpholinoaniline according to Method D1c.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841330B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-38f42cd5c9cf4714bf58274e66373df2
Quellennotizuspto-grants-2014_09