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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 241581생성일: 2026년 10월 26일

Acetone → 7-(4-Chlorobutoxy)-1,2,3,4-tetrahydroquinolin-2-one

https://huagongshe.com/reaction/241581

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물Potassium CarbonateHCID 11430—
반응물1-Bromo-4-chlorobutaneHCID 81364—
반응물7-Hydroxy-3,4-dihydrocarbostyrilHCID 2785758—
용매HexaneHCID 8058—
생성물7-(4-Chlorobutoxy)-1,2,3,4-tetrahydroquinolin-2-oneHCID 1046746778%

반응 단계

1-bromo-4-chloro-butane (3.4 g, 20 mmol), anhydrous potassium carbonate powder (4.14 g, 30 mmol) and 7-hydroxy-3,4-dihydro-2(1H)-quinolinone (1.63 g, 10 mmol) are added to 10 ml of acetone and reflux for 24 hours. The reaction solution is evaporated to dryness and dispersed with 20 ml of dichloromethane and 20 ml of water respectively. The organic layer is extracted with water (20 ml×2) and saturated saline (20 ml) successively, dried over anhydrous magnesium sulfate, and evaporated to dryness, to obtain a light yellow powder. The resulting powder is slurried with n-hexane (20 ml×3), filtered, and dried to obtain 1.98 g of 7-(4-chlorobutoxy)-3,4-dihydro-2(1H)-quinolinone, with a yield of 78%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653069B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-fb3ae03c07f64429af56703797c27a50
출처 메모uspto-grants-2014_02