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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 279399생성일: 2026년 10월 25일

8-Hydroxyquinoline → Aluminium tri(quinolin-8-olate)

https://huagongshe.com/reaction/279399

반응식

참여 물질

역할이름HCID투입량
반응물8-HydroxyquinolineHCID 1923—
반응물Aluminum StearateHCID 12496—
용매TolueneHCID 1140—
생성물Aluminium tri(quinolin-8-olate)HCID 90594—

반응 단계

Aluminum stearate, Al[CH3(CH2)16CO2]3, (10.0 g, Fisher Scientific Co., Pittsburgh, Pa., technical grade) was placed in a 250 mL round bottomed flask equipped with a magnetic stir bar and a reflux condenser. Toluene (50 mL) was added to give a white slurry. Separately, a 6.0 g sample of 8-hydroxyquinoline (41.3 mmol) was dissolved in 150 mL of toluene and the solution was gravity filtered through a coarse glass frit into the reaction flask. This removed an insoluble minor impurity found in the 8-hydroxyquinoline. After the addition of the 8-hydroxyquinoline to the aluminum stearate-toluene solution, the reaction flask was heated to reflux by means of an electric heating mantle. As the reaction warmed, but prior to refluxing, a large quantity of a fine yellow solid precipitated. The reaction mixture was refluxed for approximately 72 hours, cooled, and filtered. The yellow filter cake was washed sequentially with two 50 mL portions of toluene and two 50 mL portions of petroleum ether. After vacuum drying, the filter cake provided 5.4 g of tris(8-quinolinolato)aluminum as fine yellow needles. An 1H-NMR of the product precipitated from the toluene reaction mixture showed no significant resonances other than those of the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06362339B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-92d5daa74753410283ff95efb4551314
출처 메모uspto-grants-2002_03