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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7141Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/7141

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
PatentnummerUS07084155B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-ea0c4929da2f428f81be0a64ddc30905
Quellennotizuspto-grants-2006_08