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HRID 406482作成日:2026年10月24日

Ethyl iodoacetate → (1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-acetic acid ethyl ester

https://huagongshe.com/ja/reaction/406482

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl iodoacetateHCID 12183—
反応物Sodium hydrideHCID 24758—
反応物3,4-dihydroisoquinolin-1(2H)-oneHCID 150896—
溶媒TolueneHCID 1140—
生成物(1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-acetic acid ethyl esterHCID 59764846—

反応手順

To a solution of 3,4-dihydro-2H-isoquinolin-1-one (0.250 g, 1.70 mmol) in toluene (5 mL) was added sodium hydride (60% in mineral oil, 0.049 g, 2.04 mmol) and the resulting suspension was heated at about reflux for about 1 h. The reaction mixture was cooled at room temperature and ethyl 2-iodoacetate (0.364 g, 1.70 mmol) was added dropwise and the mixture was again heated at about reflux for about 12 h. The reaction mixture was cooled at room temperature and filtered, rinsed with toluene. The filtrate was concentrated in vacuo to provide (1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-acetic acid ethyl ester as a peach oil (0.336 g, 1.44 mmol). The crude material was used in subsequent reactions without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08754107B2
出典データセットuspto-grants-2014_06
ORD IDord-1d1de92b70de414f8fecb0ebfe936e74
出典メモuspto-grants-2014_06