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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2416592생성일: 2026년 10월 26일

Ethanol → 4,5-Dimethoxy-2-(4-methylthiophenyl)benzaldehyde

https://huagongshe.com/reaction/2416592

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Sodium CarbonateHCID 10340—
반응물2-Bromo-3,4-dimethoxybenzaldehydeHCID 618538—
반응물4-(Methylthio)phenylboronic acidHCID 2733959—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물4,5-Dimethoxy-2-(4-methylthiophenyl)benzaldehydeHCID 1139208085%

반응 단계

2-Bromoveratraldehyde (25 g, 103.3 mmol) and 4-(methylthio)benzeneboronic acid (19.66 g, 118.5 mmol) were dissolved in toluene (550 mL) and sodium carbonate (2M, 103 μL, 206 mmol) was added. To this reaction mixture was added ethanol (50 mL) followed by tetrakis (triphenylphosphine)palladium (3.4 g, 2.5 mmol) and the reaction mixture was refluxed overnight under nitrogen atmosphere. The reaction mixture was cooled to room temperature, diluted with water (250 mL) and extracted with ethyl acetate (2×250 mL). The combined organic extracts were washed with water (4×250 mL), brine (1×250 mL), dried over sodium sulfate, filtered and the filtrate was evaporated under reduced pressure to give the crude product. The product was purified by trituration with ethyl acetate/hexane to give the title compound as a white solid (21.3 g, 85% yield), mp 114-115° C. 1H NMR (CDCl3, 300 MHz) δ 9.83 (s, 1H), 7.64 (s, 1H), 7.43-7.23 (m, 4H), 6.83 (s, 1H), 3.98 (d, J=2.4 Hz, 6H), 2.55 (s, 3H). 13C NMR (CDCl3, 75.45 MHz) δ 190.9, 153.4, 148.7, 1408, 138.9, 134.5, 134.1, 130.5, 130.1, 128.0, 128.0, 126.9, 126.1, 112.5, 108.7, 56.2, 56.1, 15.6. LRMS (APIMS) m/z 289 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06825185B2
출처 데이터셋uspto-grants-2004_11
ORD IDord-37e15bee1d2b488ea0e7f19945ea824b
출처 메모uspto-grants-2004_11