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HRID 49185생성일: 2026년 10월 24일

Potassium Hydroxide → 7-(2-Chlorophenyl)-4-methyl-5,6,7,8-tetrahydroquinolin-5-one

https://huagongshe.com/ko/reaction/49185

반응식

참여 물질

역할이름HCID투입량
반응물Potassium HydroxideHCID 14797—
반응물4,4-Dimethoxy-2-butanoneHCID 228548—
반응물1-Amino-5-(2-chlorophenyl)cyclohexen-3-oneHCID 9859316—
용매EthanolHCID 702—
용매TolueneHCID 1140—
생성물7-(2-Chlorophenyl)-4-methyl-5,6,7,8-tetrahydroquinolin-5-oneHCID 1106556175.5%

반응 단계

A solution of 1-amino-5-(2-chlorophenyl)cyclohexen-3-one (2.7 g) in ethanol (50 ml) and toluene (150 m) was combined with acetyl acetoaldehyde dimethyl acetal (4.0 g) and 85% potassium hydroxide (0.67 g), and the mixture was heated under reflux. 85% Potassium hydroxide (0.14 g) was added three times at an interval of 30 minutes, and then heated under reflux further for 1 hour. The solvent was distilled off under reduced pressure, and the residue was combined with ethyl acetate, washed successively with water and saturated brine, and dried over magnesium sulfate. After concentrating under reduced pressure, the residue was subjected to a column chromatography on a silica gel (EtOAc-hexane) to obtain 7-(2-chlorophenyl)-4-methyl-5,6,7,8-tetrahydroquinolin-5-one (2.5 g) as a crystal. Melting point and NMR data were in agreement with those of the compound obtained in Reference Example 2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706732B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-25a6346f6a0b46519b1f9908d027fc48
출처 메모uspto-grants-2004_03