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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 35689Erstellt: 24. Oktober 2026

4-(4-Chlorophenoxy)aniline → HCID 70408543, Verbindung

https://huagongshe.com/de/reaction/35689

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-(4-Chlorophenoxy)anilineHCID 7578—
EduktDiphosgeneHCID 10426—
Edukt3-(4-Chlorophenyl)-4-phenylpyrazolineHCID 70409590—
KatalysatorTriethylamineHCID 8471—
LösungsmittelTolueneHCID 1140—
LösungsmittelDiethyl EtherHCID 3283—
ProduktHCID 70408543HCID 7040854353,9%

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

To a stirred solution of 0.75 g (0.0034 mole) 4-(4-chlorophenoxy)aniline in 25 mL of toluene was added dropwise a solution of 0.43 mL (0.0036 mole) trichloromethylchloroformate in 20 mL of toluene. After complete addition, the mixture was heated at 85° C. for three hours. This mixture was cooled to room temperature and the solvent evaporated under reduced pressure to leave a residue. The residue was dissolved in 25 mL of diethyl ether. This solution was added dropwise to a stirred slurry of 1.0 g (0.0034 mole) of 3-(4-chlorophenyl)-4-phenylpyrazoline in diethyl ether. Three drops of triethylamine were added and the mixture was stirred at room temperature for two days. The solvent was evaporated from the mixture to yield 0.92 g of 3-(4-chlorophenyl)-N-[4-(4-chlorophenoxy)phenyl]-4-phenylpyrazoline-1-carboxamide (mp 158°-161° C.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04767779
Quelldatensatzuspto-grants-1988_08
ORD IDord-0c0d0a5e79614c0a9f11be0474df246f
Quellennotizuspto-grants-1988_08