Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7084Erstellt: 23. Oktober 2026

Benzaldehyde → 4-hydroxy-3-methoxy-N-[1-oxo-2-phenylmethylidene-1,2,3,4-tetrahydronaphthalen-7-yl]phenylacetamide

https://huagongshe.com/de/reaction/7084

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
Edukt7-Amino-1,2,3,4-tetrahydronaphthalen-1-oneHCID 327177—
Edukt3-(Cyclohexen-1-yl)anilineHCID 6709749—
Edukt4-hydroxy-3-methoxy-N-[1-oxo-1,2,3,4-tetrahydronaphthalen-7-yl]phenylacetamideHCID 22019659—
LösungsmittelEthanol hydrochlorideHCID 21887872—
Produkt4-hydroxy-3-methoxy-N-[1-oxo-2-phenylmethylidene-1,2,3,4-tetrahydronaphthalen-7-yl]phenylacetamideHCID 69663967—

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

Instead of 3-(cyclohexen-1-yl)aniline (Intermediate 2) in Example 9, 7-amino-1-tetralone is treated in a similar manner to Example 9. The resulting 4-hydroxy-3-methoxy-N-[1-oxo-1,2,3,4-tetrahydronaphthalen-7-yl]phenylacetamide (1 g) is dissolved in 30% hydrogen chloride-ethanol (5 ml), and thereto is added benzaldehyde (433 mg). The mixture is stirred at 25° C. for 18 hours. The precipitated crystals are collected by filtration, and washed with diethyl ether to give the desired compound (700 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07084176B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-18b1747dcc8a42479959da4aec8199c0
Quellennotizuspto-grants-2006_08