돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 271832생성일: 2026년 10월 26일

3-Benzyl-7-chloroquinoline-2-carbaldehyde → 1-(3-Benzyl-7-chloroquinolin-2-yl)-2-methylpropan-1-ol

https://huagongshe.com/reaction/271832

반응식

참여 물질

역할이름HCID투입량
반응물3-Benzyl-7-chloroquinoline-2-carbaldehydeHCID 59836197—
반응물HCID 178418918HCID 178418918—
용매DichloromethaneHCID 6344—
생성물1-(3-Benzyl-7-chloroquinolin-2-yl)-2-methylpropan-1-olHCID 5983619130%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07452996B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-38bebffedd004238a9d7d4ab96442a31
출처 메모uspto-grants-2008_11