Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Thioanisole → 2-[(heptylsulfanyl)methyl]-3-methylquinolin-4(1H)-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Thioanisole | HCID 7520 | — |
| 반응물 | 4-(Benzyloxy)-2-[(heptylsulfanyl)methyl]-3-methylquinoline | HCID 59527296 | — |
| 용매 | Trifluoroacetic acid | HCID 6422 | — |
| 생성물 | 2-[(heptylsulfanyl)methyl]-3-methylquinolin-4(1H)-one | HCID 59527255 | 95.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08367702B2 |
| 출처 데이터셋 | uspto-grants-2013_02 |
| ORD ID | ord-7d10b21b5f264ec59469e3058e13c6d9 |
| 출처 메모 | uspto-grants-2013_02 |