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HRID 271832作成日:2026年10月26日

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

https://huagongshe.com/reaction/271832

反応式

関与物質

役割名称HCID仕込み量
反応物3-Benzyl-7-chloroquinoline-2-carbaldehydeHCID 59836197—
反応物HCID 178418918HCID 178418918—
溶媒DichloromethaneHCID 6344—
生成物1-(3-Benzyl-7-chloroquinolin-2-yl)-2-methylpropan-1-olHCID 5983619130%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07452996B2
出典データセットuspto-grants-2008_11
ORD IDord-38bebffedd004238a9d7d4ab96442a31
出典メモuspto-grants-2008_11