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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7141생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물4-CyanobenzaldehydeHCID 66042—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물8-Amino-5,6,7,8-tetrahydroquinolineHCID 11355564—
용매DichloromethaneHCID 6344—
생성물N-(5,6,7,8-tetrahydro-8-quinolinyl)-4-cyanobenzylamineHCID 2201853272%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084155B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-ea0c4929da2f428f81be0a64ddc30905
출처 메모uspto-grants-2006_08