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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 488819생성일: 2026년 10월 26일

Water → 3-(1,4-Diisopropyl-6-methyl-1,2,3,4-tetrahydro-7-quinoxalinyl)-4-methoxybenzaldehyde

https://huagongshe.com/reaction/488819

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물5-Formyl-2-methoxyphenylboronic acidHCID 2734367—
반응물7-Bromo-1,4-diisopropyl-6-methyl-1,2,3,4-tetrahydroquinoxalineHCID 22268301—
촉매HCID 178418397HCID 178418397—
용매1,2-DimethoxyethaneHCID 8071—
생성물3-(1,4-Diisopropyl-6-methyl-1,2,3,4-tetrahydro-7-quinoxalinyl)-4-methoxybenzaldehydeHCID 22268343—

반응 단계

A mixture of 7-bromo-1,4-diisopropyl-6-methyl-1,2,3,4-tetrahydroquinoxaline (469 mg, 1.51 mmol), 2-methoxy-5-formylphenylboronic acid (407 mg, 2.26 mmol), potassium carbonate (834 mg, 6.03 mmol) and water (2.5 mL) in anhydrous 1,2-dimethoxyethane (30 mL) was degassed with argon for 15 minutes prior to the addition of tetrakis(triphenylphosphine)palladium (0) (349 mg, 0.30 mmol). The reaction mixture was heated under reflux for 8.5 hours, allowed to cool to room temperature and extracted with ethyl acetate (2×100 mL). The organic extracts were successively washed with water (100 mL), saturated aqueous NH4Cl (100 mL), saturated aqueous NaCl (100 mL), dried over MgSO4 and filtered. Removal of the solvent under reduced pressure gave an oil which was purified by column chromatography, using a Biotage 40S cartridge, eluting with 10% ethyl acetate/90% hexane. The title compound was isolated as bright yellow solid (315 mg, 57%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06974826B2
출처 데이터셋uspto-grants-2005_12
ORD IDord-8c7b368876644e1d9de9d4b20aac2b9d
출처 메모uspto-grants-2005_12