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HRID 33864作成日:2026年10月24日

Methyl Benzoate → 4-(2-Quinolin-2-yl-ethyl)-benzoic acid methyl ester

https://huagongshe.com/ja/reaction/33864

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl BenzoateHCID 7150—
反応物TetrahydrofuranHCID 8028—
反応物Sodium hydrideHCID 24758—
反応物2-QuinolinecarboxaldehydeHCID 79619—
触媒Palladium hydroxideHCID 9942167—
溶媒EthanolHCID 702—
生成物4-(2-Quinolin-2-yl-ethyl)-benzoic acid methyl esterHCID 68575869—

反応手順

To a solution of 4-[Triphenyl-phophanyl)-methyl]-benzoic acid methyl ester (1.87 g) in THF (16 ml) under N2 atmosphere at 0° C. was added sodium hydride (165 mg (60%)). After 30 min, quinoline-2-carbaldehyde (0.50 g) was added and the reaction stirred at ambient temperature for 2 h. The reaction mixture was quenched with brine, extracted with chloroform, dried magnesium sulfate, filtered and concentrated to provide the crude alkene. The crude product was placed on a parr shaker in ethanol (15 ml) with palladium hydroxide (200 mg) as the catalyst under 10 PSI of H2. After 40 min, the reaction mixture was filtered through celite and concentrated. Biotage MPLC chromatography eluting with 10-20% ethyl acetate/hexane provided the title compound. MS: (M+H m/z=292.1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07429665B2
出典データセットuspto-grants-2008_09
ORD IDord-68e438b175834339a48d1f36eaa20468
出典メモuspto-grants-2008_09