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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 384489생성일: 2026년 10월 25일

Thioanisole → 2-[(heptylsulfanyl)methyl]-3-methylquinolin-4(1H)-one

https://huagongshe.com/reaction/384489

반응식

참여 물질

역할이름HCID투입량
반응물ThioanisoleHCID 7520—
반응물4-(Benzyloxy)-2-[(heptylsulfanyl)methyl]-3-methylquinolineHCID 59527296—
용매Trifluoroacetic acidHCID 6422—
생성물2-[(heptylsulfanyl)methyl]-3-methylquinolin-4(1H)-oneHCID 5952725595.1%

반응 단계

To a solution of 4-(benzyloxy)-2-[(heptylsulfanyl)methyl]-3-methylquinoline (150 mg) in trifluoroacetic acid (5 mL) was added thioanisole (150 mg), followed by stirring at room temperature for 16 hours. The reaction mixture was added dropwise to an ice-cold aqueous sodium hydrogen carbonate solution, followed by extraction with ethyl acetate (50 mL). The organic layer was washed with saturated brine, and then dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: chloroform/methanol=10/1) to obtain 2-[(heptylsulfanyl)methyl]-3-methylquinolin-4(1H)-one (110 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367702B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-7d10b21b5f264ec59469e3058e13c6d9
출처 메모uspto-grants-2013_02