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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8711생성일: 2026년 10월 24일

Ethyl Acetate → alpha-(5-BRomo-1,3-benzodioxol-4-yl)-5-isoquinolinemethanol

https://huagongshe.com/ko/reaction/8711

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물1-Bromo-3,4-(methylenedioxy)benzeneHCID 75831—
반응물Lithium diisopropylamideHCID 2724682—
반응물Isoquinoline-5-carboxaldehydeHCID 7016853—
용매TetrahydrofuranHCID 8028—
생성물alpha-(5-BRomo-1,3-benzodioxol-4-yl)-5-isoquinolinemethanolHCID 1098120065%

반응 조건

온도-78 °C

반응 단계

To a solution of 4-bromo-1,2-(methylendioxy)benzene (3.01 g, 15 mmol) in THF (20 mL) at −78° C. was added dropwise lithium diisopropylamide (10.6 mL of 1.5 M in cyclohexane, 16 mmol). The reaction mixture was stirred at −78° C. under argon for 20 minutes. A brown solution was formed. A solution of 5-isoquinolinecarboxaldehyde (1.90 g, 12 mmol) in THF (4 mL) was added dropwise. The resulting mixture was stirred at −78° C. for 10 minutes and warmed to room temperature. Stirring was continued for 30 minutes at room temperature, and then the mixture was quenched with saturated NH4Cl solution. The product was extracted with EtOAc and the solvent was removed under reduced pressure. Chromatography (SiO2 Type-H, 35% EtOAc in Hexanes) of the residue yielded the title compound as a yellow solid (2.8 g, 7.8 mmol, 65% yield): mp 173–175° C.;

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091212B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-d7ba93572fa64fddbb46271e8f729e27
출처 메모uspto-grants-2006_08