Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Sodium Hydroxide → 4-(Benzyloxy)-2-[(heptylsulfinyl)methyl]-3-methylquinoline
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | m-Chloroperbenzoic acid | HCID 70297 | — |
| 반응물 | 4-(Benzyloxy)-2-[(heptylsulfanyl)methyl]-3-methylquinoline | HCID 59527296 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-(Benzyloxy)-2-[(heptylsulfinyl)methyl]-3-methylquinoline | HCID 59527314 | 68% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08367702B2 |
| 출처 데이터셋 | uspto-grants-2013_02 |
| ORD ID | ord-d58d66f255d94c5cbadca1ba63e3abc4 |
| 출처 메모 | uspto-grants-2013_02 |