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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 384441생성일: 2026년 10월 26일

1-Heptanethiol → 4-(Benzyloxy)-2-[(heptylsulfanyl)methyl]-3-methylquinoline

https://huagongshe.com/reaction/384441

반응식

참여 물질

역할이름HCID투입량
반응물1-HeptanethiolHCID 15422—
반응물p-Toluenesulfonic acid [4-(benzyloxy)-3-methylquinolin-2-yl]methyl esterHCID 59527351—
용매MethanolHCID 887—
용매Sodium MethoxideHCID 10942334—
용매MeOH tetrahydrofuranHCID 21899815—
생성물4-(Benzyloxy)-2-[(heptylsulfanyl)methyl]-3-methylquinolineHCID 5952729690.2%

반응 단계

1-Heptanethiol (250 mg) was dissolved in methanol (5 mL), to which a solution of 28% sodium methoxide in methanol (0.37 mL) was then added, followed by stirring at room temperature for 15 minutes. The reaction mixture was added to a solution of p-toluenesulfonic acid [4-(benzyloxy)-3-methylquinolin-2-yl]methyl ester (464 mg) in methanol-THF (1:1, 10 mL), followed by stirring at room temperature for 30 minutes. The reaction mixture was concentrated under reduced pressure, and water (100 mL) was added to the resulting residue, followed by extraction with ethyl acetate (100 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: hexane/ethyl acetate=5/1) to obtain 4-(benzyloxy)-2-[(heptylsulfanyl)methyl]-3-methylquinoline (380 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367702B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-dad718cd7b364c2096a6aefe1577d3a2
출처 메모uspto-grants-2013_02