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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1921572생성일: 2026년 10월 26일

Acetic Acid → [(3-Methoxyphenyl)methylene]-2-methylquinolin-5-amine

https://huagongshe.com/reaction/1921572

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물WaterHCID 962—
반응물3-MethoxybenzaldehydeHCID 11569—
반응물5-Quinolinamine, 2-methyl-HCID 148683—
용매TolueneHCID 1140—
생성물[(3-Methoxyphenyl)methylene]-2-methylquinolin-5-amineHCID 67136368102.7%

반응 단계

To 1.17 g (7.4 mmol) 5-amino-2-methylquinolin and 1 g (7.4 mmol) 3-methoxybenzaldehyde in 39 ml toluene are added 1 ml acetic acid. The mixture is heated over 3 hours under reflux while water is trapped in a Dean Stark apparatus. The solvent is evaporated and the residue is two times azeotrophed with small portions of toluene. 2.1 g of [(3-methoxyphenyl)methylene]-2-methylquinolin-5-amine are obtained as product. 0.31 ml (3.6 mmol) 1,1,1-trifluoroepoxypropane in 17 ml THF and are cooled to −104° C. and 1.59 ml of a 2.5 M n-butyl lithium solution in hexane are added over 3 hours while the temperature does not exceed −99° C. 10 Minutes after complete addition 1.5 g (5.4 mmol) [(3-methoxyphenyl)methylene]-2-methylquinolin-5-amine in 5 ml THF are added over 0.5 hours while the temperature temperature does not exceed −99° C. After 0.5 hours at −100° C. 4 ml diethyl ether are added and the reaction mixture is warmed to 20° C. over one hour. The reaction was quenched by addition of saturated ammonium chloride solution. The phases were separated and the aqueous layer was extracted twice with diethyl ether, the combined organic phases washed with brine, dried over sodium sulphate and then evaporated. Flash chromatography on silica gel (aceton in hexane 30 to 40%) yields 800 mg of the desired epoxide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08173676B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-82dfa9a583fb44ecbf1e9153569148c6
출처 메모uspto-grants-2012_05