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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 78372Erstellt: 23. Oktober 2026

Tetrahydrofurfurylamine → 3-(4-Nitrophenoxy)benzoic acid

https://huagongshe.com/de/reaction/78372

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofurfurylamineHCID 253298—
Edukt3-(4-Nitrophenoxy)benzoic acidHCID 767919—
Produkt3-(4-Nitrophenoxy)benzoic acidHCID 767919—
Produkt3-(4-nitrophenoxy)-N-(tetrahydro-2-furanylmethyl)benzamideHCID 2986507—

Reaktionsschritte

Entry 63: 4-(3-Carboxyphenoxy)-1-nitrobenzene was synthesized according to Method A13, Step 2. 4-(3-Carboxyphenoxy)-1-nitrobenzene was coupled with tetrahydrofurfurylamine according to Method A13, Step 3 to give 4-(3-(N-(tetrahydrofurylmethyl)carbamoyl)phenoxy)-1-nitrobenzene. According to Method A13 Step 4, 4-(3-(N-(tetrahydrofurylmethyl)carbamoyl)phenoxy)-1-nitrobenzene was reduced to 4-(3-(N-(tetrahydrofurylmethyl)carbamoyl)phenoxy)aniline. According to Method C1a, 4-chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(3-(N-(tetrahydrofurylmethyl)carbamoyl)phenoxy)aniline to afford the urea.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841330B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-960654546b55426a858bdc82374e4060
Quellennotizuspto-grants-2014_09