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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1673262생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1673262

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 번호US07999108B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-4c2ae1de66fc4d98a4716ddc42922fb5
출처 메모uspto-grants-2011_08