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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1835598생성일: 2026년 10월 26일

Aluminum(III) Chloride → 1-Amino-6-[(4,6-diphenyl-2-pyridinyl)oxy]-hexane

https://huagongshe.com/reaction/1835598

반응식

참여 물질

역할이름HCID투입량
반응물Aluminum(III) ChlorideHCID 6451240—
반응물6-[(4,6-Diphenyl-2-pyridyl)oxy]hexanonitrileHCID 10337448—
반응물Aluminium lithium hydrideHCID 21226445—
용매Diethyl EtherHCID 3283—
생성물1-Amino-6-[(4,6-diphenyl-2-pyridinyl)oxy]-hexaneHCID 2350167071%

반응 단계

To a dry flask was added aluminum chloride (0.857 g, 6.42 mmol). The flask was cooled to less than 0° C. with an ice/ethanol bath. Ether (15 mL) was added, and the reaction was stirred for 5 min until the aluminum chloride dissolved. Lithium aluminum hydride (0.244 g, 6.42 mmol) was then added, and the reaction was heated to reflux. 6-[(4,6-Diphenyl-2-pyridinyl)oxy]-hexanenitrile (1.0 g, 2.92 mmol) was dissolved in ether (5 mL) and added dropwise to the refluxing solution. After addition was complete, the reaction was stirred overnight at room temperature. The reaction was then quenched with water. 6 N Aqueous sulfuric acid was added until a clear solution formed. This mixture was then extracted with ether (3×). The aqueous layer was then cooled in an ice bath and basified to pH 14 with 50% aq. NaOH. This was then extracted with ether (4×). The organic layer was then washed with saturated NaCl, dried over magnesium sulfate, and evaporated to give 0.7184 g (71%) of 1-amino-6-[(4,6-diphenyl-2-pyridinyl)oxy]-hexane as an oil. ESMS: Calcd. For C23H26N2O, 346.20; Found, 347.3 (M+H)+1

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06770259B2
출처 데이터셋uspto-grants-2004_08
ORD IDord-6a23193eca314f6c8e8f34f57fef43bb
출처 메모uspto-grants-2004_08