Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
3-Benzyl-7-chloroquinoline-2-carbaldehyde → 1-(3-Benzyl-7-chloroquinolin-2-yl)-2-methylpropan-1-ol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 3-Benzyl-7-chloroquinoline-2-carbaldehyde | HCID 59836197 | — |
| 반응물 | HCID 178418918 | HCID 178418918 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 1-(3-Benzyl-7-chloroquinolin-2-yl)-2-methylpropan-1-ol | HCID 59836191 | 30% |
반응 단계
To a solution of 3-benzyl-7-chloroquinoline-2-carbaldehyde (1.23 g, 4.4 mmol) in anhydrous DCM (12 ml) at −78° C., was added isopropylmagnesium chloride (6.6 m, 13.2 mmol). The resulting solution was allowed to warm to ambient temperature over one hour. The reaction mixture was then quenched with saturated NH4Cl and extracted with DCM (3×). The combined organic layers were washed with brine, dried over MgSO4, and the solvent was removed in vacuo. The crude product was subjected to flash column chromatography using an ISCO purification system. Elution in hexanes with a gradient of ethyl acetate (0-100%) yielded 1-(3-benzyl-7-chloroquinolin-2-yl)-2-methylpropan-1-ol 25 (0.44 g, 1.3 mmol, 30%) as a red oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07452996B2 |
| 출처 데이터셋 | uspto-grants-2008_11 |
| ORD ID | ord-38bebffedd004238a9d7d4ab96442a31 |
| 출처 메모 | uspto-grants-2008_11 |