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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1192560생성일: 2026년 10월 27일

Hydrochloric Acid → 1-(8-Hydroxy-5-methylquinolin-7-yl)ethanone

https://huagongshe.com/reaction/1192560

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Acetyl chlorideHCID 6367—
반응물Sodium HydroxideHCID 14798—
반응물5-Methyl-8-hydroxyquinolineHCID 71208—
반응물Aluminum(III) ChlorideHCID 6451240—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물1-(8-Hydroxy-5-methylquinolin-7-yl)ethanoneHCID 19043459—

반응 조건

온도0 °C

반응 단계

A mixture of 5-methylquinolin-8-ol (5.91 g, 37.1 mmol, from ChemBridge), aluminum trichloride (20.00 g, 150.0 mmol), and acetyl chloride (12.1 mL, 170 mmol) was stirred at 0° C. for 4 hours, then heated at 130° C. for 12 hours, cooled, and decomposed with water (39 mL) (caution! with external ice-cooling if necessary) and conc. HCl (13 mL). The precipitate was filtered, and dried under reduced pressure. The solid obtained was then dissolved in 50 mL of water. To the solution was added 100 mL of dichloromethane. The mixture was cooled with an ice bath and the pH adjusted to 4 with slow addition of 20% NaOH. The layers were separated and the aqueous layer was extracted with dichloromethane. The combined organic layers were washed with water, brine and dried over sodium sulfate. The suspension was filtered through a plug of cotton and concentrated to dryness. The residue was used directly in the next step (5.8 g, 78%). LCMS calculated for C12H12NO2 (M+H)+: m/z=202.1; Found: 202.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08680108B2
출처 데이터셋uspto-grants-2014_03
ORD IDord-fda3c65bbef748bcb621dd751cbffa39
출처 메모uspto-grants-2014_03