HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-Methoxy-5-(trifluoromethyl)aniline → 3-(4-Aminophenoxy)benzoic acid
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-Methoxy-5-(trifluoromethyl)aniline | HCID 600637 | — |
| Edukt | Benzene, 2-isocyanato-1-methoxy-4-(trifluoromethyl)- | HCID 11983909 | — |
| Edukt | 3-(4-Aminophenoxy)benzoic acid | HCID 23009036 | — |
| Produkt | 3-(4-Aminophenoxy)benzoic acid | HCID 23009036 | — |
| Produkt | N-(5-(trifluoromethyl)-2-methoxyphenyl)-N'-(3-carboxyphenyl)urea | HCID 23614600 | — |
Reaktionsschritte
Entry 37: 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-(dimethylamino)aniline according to Method D1c.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08841330B2 |
| Quelldatensatz | uspto-grants-2014_09 |
| ORD ID | ord-13bb777dbf4045ef9deaed4294272239 |
| Quellennotiz | uspto-grants-2014_09 |