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HRID 1948728作成日:2026年10月26日

8-Methyl-2-phenylquinoline-3-carboxaldehyde → 1-(8-Methyl-2-phenylquinolin-3-yl)ethanol

https://huagongshe.com/reaction/1948728

反応式

関与物質

役割名称HCID仕込み量
反応物8-Methyl-2-phenylquinoline-3-carboxaldehydeHCID 833680—
反応物HCID 178418348HCID 178418348—
溶媒TetrahydrofuranHCID 8028—
生成物1-(8-Methyl-2-phenylquinolin-3-yl)ethanolHCID 6719775665%

反応手順

To a solution of 8-methyl-2-phenylquinoline-3-carboxaldehyde (211 mg, 0.85 mmol) in THF (6 mL) cooled to −78° C. was added methyllithium (1.6N solution in ether, 0.6 mL, 0.93 mmol). After 1 h a further portion of methyllithium (0.2 mL, 0.32 mmol) was added. The reaction was allowed to warm to r.t. before being quenched with water (10 mL). The THF was removed in vacuo and the residue partitioned between DCM (100 mL) and water (30 mL). The organic layer was separated, dried (MgSO4) and concentrated in vacuo. Purification by column chromatography (SiO2, 5-25% EtOAc in heptane) gave the title compound as a white solid (145 mg, 65%). δH (CDCl3) 8.42 (s, 1H), 7.70 (d, J 12 Hz, 1H), 7.60-7.63 (m, 2H), 7.42-7.55 (m, 5H), 5.23-5.31 (m, 1H), 2.80 (s, 3H), 1.87 (d, J 3.6 Hz, 1H), 1.47 (d, J 6.4 Hz, 3H). LCMS (ES+) 264.16 (M+H)+, RT 4.03 minutes (Method 4).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08399483B2
出典データセットuspto-grants-2013_03
ORD IDord-28319f5592994a859bd5d9a8b0630a8e
出典メモuspto-grants-2013_03