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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 406482생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/406482

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl iodoacetateHCID 12183—
반응물Sodium hydrideHCID 24758—
반응물3,4-dihydroisoquinolin-1(2H)-oneHCID 150896—
용매TolueneHCID 1140—
생성물(1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-acetic acid ethyl esterHCID 59764846—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08754107B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-1d1de92b70de414f8fecb0ebfe936e74
출처 메모uspto-grants-2014_06