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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 384442생성일: 2026년 10월 25일

Sodium Hydroxide → 4-(Benzyloxy)-2-[(heptylsulfinyl)methyl]-3-methylquinoline

https://huagongshe.com/reaction/384442

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물m-Chloroperbenzoic acidHCID 70297—
반응물4-(Benzyloxy)-2-[(heptylsulfanyl)methyl]-3-methylquinolineHCID 59527296—
용매DichloromethaneHCID 6344—
생성물4-(Benzyloxy)-2-[(heptylsulfinyl)methyl]-3-methylquinolineHCID 5952731468%

반응 단계

To a solution of 4-(benzyloxy)-2-[(heptylsulfanyl)methyl]-3-methylquinoline (106 mg) in dichloromethane (5 mL) was added m-chloroperbenzoic acid (75%, 68 mg) at −30° C., followed by stirring for 5 hours while warming to room temperature. A 0.2M aqueous sodium hydroxide solution (20 mL) was added to the reaction mixture, followed by extraction with chloroform (50 mL). The organic layer was washed sequentially with water and saturated brine and then dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: chloroform/methanol=10/1) to obtain 4-(benzyloxy)-2-[(heptylsulfinyl)methyl]-3-methylquinoline (75 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367702B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-d58d66f255d94c5cbadca1ba63e3abc4
출처 메모uspto-grants-2013_02