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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7141Generated: October 23, 2026

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

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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-CyanobenzaldehydeHCID 66042—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant8-Amino-5,6,7,8-tetrahydroquinolineHCID 11355564—
SolventDichloromethaneHCID 6344—
ProductN-(5,6,7,8-tetrahydro-8-quinolinyl)-4-cyanobenzylamineHCID 2201853272%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084155B2
Source datasetuspto-grants-2006_08
ORD IDord-ea0c4929da2f428f81be0a64ddc30905
Source noteuspto-grants-2006_08