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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10743생성일: 2026년 10월 25일

Hydrogen Peroxide → 2,4-dimethoxy-5-(1-methyl-1H-indol-2-yl)benzaldehyde

https://huagongshe.com/reaction/10743

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물TriethylboraneHCID 7357—
반응물1-MethylindoleHCID 11781—
반응물Sodium HydroxideHCID 14798—
반응물5-Bromo-2,4-dimethoxybenzaldehydeHCID 668346—
반응물HCID 178418306HCID 178418306—
촉매HCID 178418476HCID 178418476—
용매TetrahydrofuranHCID 8028—
생성물2,4-dimethoxy-5-(1-methyl-1H-indol-2-yl)benzaldehydeHCID 2198100625%

반응 단계

Ex-116A: To a solution of N-methyl indole (1.3 g, 10 mmol) in 50 ml THF, t-BuLi (1.7 m in THF, 7.1 ml, 12 mmol) was slowly added at 0° C. under nitrogen. The mixture was stirred at room temperature for 1 hr, BEt3 (1.0 M in THF, 12 ml, 12 mmol) was added, and the mixture stirred for another 1 hr at room temperature. Then, PdCl2(PPh3)2 (0.35 g, 0.5 mmol) and 5-bromo-2,4-dimethoxybenzaldehyde (3.7 g, 15 mmol) were added, and the mixture was heated to about 60° C. for 30 minutes. The reaction mixture was poured into 50 ml 10% NaOH and treated with 30% H2O2 and then stirred for 10 minutes. The mixture was extracted with EtOAc and combined organic phase was washed with H2O and brine, dried over MgSO4, and absorbed to small amount of silica gel. Column chromatography (EtOAc:Hexane, 1:2) gave 0.72 g (25%) 2,4-dimethoxy-5-(1-methyl-1H-indol-2-yl)-benzaldehyde. 1H-NMR (CDCl3) δ 10.33 (s, 1H), 7.84 (s, 1H), 7.60 (d, J=8 Hz, 1H), 7.31 (d, J=8 Hz, 1H), 7.18–7.24 (m, 1H), 7.07–7.12 (m, 1H), 6.53 (s, 1H), 6.46 (s, 1H), 4.00 (s, 3H), 3.89 (s, 3H), 3.53 (s, 3H). HRMS (EI) Calcd. for C18H17NO3: 295.1208. Found: 295.1202.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094801B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-b835e6a7a7f3491a9842d10f3e2224da
출처 메모uspto-grants-2006_08