戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 747340作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物4-CyanobenzaldehydeHCID 66042—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物8-Amino-5,6,7,8-tetrahydroquinolineHCID 11355564—
溶媒DichloromethaneHCID 6344—
生成物N-(5,6,7,8-tetrahydro-8-quinolinyl)-4-cyanobenzylamineHCID 2201853272%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07396840B2
出典データセットuspto-grants-2008_07
ORD IDord-bc49d1524049415289a652d0e103bd90
出典メモuspto-grants-2008_07