Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 747340Erstellt: 23. Oktober 2026

4-Cyanobenzaldehyde → N-(5,6,7,8-tetrahydro-8-quinolinyl)-4-cyanobenzylamine

https://huagongshe.com/de/reaction/747340

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-CyanobenzaldehydeHCID 66042—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt8-Amino-5,6,7,8-tetrahydroquinolineHCID 11355564—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(5,6,7,8-tetrahydro-8-quinolinyl)-4-cyanobenzylamineHCID 2201853272%

Reaktionsschritte

To a stirred solution of 8-amino-5,6,7,8-tetrahydroquinoline (24.3 g, 164 mmol) in dichloromethane (600 mL), at room temperature, was added 4-cyanobenzaldehyde (21.5 g, 164 mmol) and sodium triacetoxyborohydride (45 g, 210 mmol). After 42 hours, the reaction was quenched with 1N NaOH (250 mL). The phases were separated and the organic phase was washed once with brine (200 mL), dried (Na2SO4), and concentrated. Purification of the crude material by flash chromatography on silica gel (5% CH3OH/CH2Cl2) provided 30.9 g (72%) of N-(5,6,7,8-tetrahydro-8-quinolinyl)-4-cyanobenzylamine as a pale yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07396840B2
Quelldatensatzuspto-grants-2008_07
ORD IDord-bc49d1524049415289a652d0e103bd90
Quellennotizuspto-grants-2008_07