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HRID 10743作成日:2026年10月26日

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

https://huagongshe.com/reaction/10743

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen PeroxideHCID 784—
反応物TriethylboraneHCID 7357—
反応物1-MethylindoleHCID 11781—
反応物Sodium HydroxideHCID 14798—
反応物5-Bromo-2,4-dimethoxybenzaldehydeHCID 668346—
反応物HCID 178418306HCID 178418306—
触媒HCID 178418476HCID 178418476—
溶媒TetrahydrofuranHCID 8028—
生成物2,4-dimethoxy-5-(1-methyl-1H-indol-2-yl)benzaldehydeHCID 2198100625%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094801B2
出典データセットuspto-grants-2006_08
ORD IDord-b835e6a7a7f3491a9842d10f3e2224da
出典メモuspto-grants-2006_08