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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 325036Erstellt: 25. Oktober 2026

Ethyl Acetate → Amino-5-[2-(4-cyanophenyl)ethoxy]-2-methylbenzene

https://huagongshe.com/reaction/325036

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktSodium borohydrideHCID 4311764—
Edukt[2-(4-Cyanophenyl)ethoxy]-4-methyl-3-nitrobenzeneHCID 22033464—
KatalysatorCopper SulfateHCID 24462—
LösungsmittelEthanolHCID 702—
ProduktAmino-5-[2-(4-cyanophenyl)ethoxy]-2-methylbenzeneHCID 2203353226%

Reaktionsschritte

Sodium borohydride (0.127 g; 3.35 mmol) was added in portions to a cold suspension (ice:water temperature) of [2-(4-cyanophenyl)ethoxy]-4-methyl-3-nitrobenzene (0.19 g; 0.67 mmol; from step (i) above) and aqueous copper sulfate (1.34 mL; 1M; 1.34 mmol) in EtOH (5 mL) over five minutes. The temperature was allowed to rise to ambient and the stirring continued for 30 minutes. Addition of EtOAc (50 mL) and filtration through Celite afforded a clear solution that was washed with water, dried (K3CO3) and concentrated in vacuo. Flash chromatography (SiO2; toluene:EtOAc (10:1)) afforded 0.044 g (26%) of the sub-title compound as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06221898B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-5390921ce5604507a4fc60d24bcec0d9
Quellennotizuspto-grants-2001_04