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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10618생성일: 2026년 10월 25일

Water → 5-Benzo[b]thiophen-2-yl-2,4-dimethoxy-benzaldehyde

https://huagongshe.com/reaction/10618

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Benzo(B)Thiophene-2-Boronic AcidHCID 2359—
반응물Sodium CarbonateHCID 10340—
반응물5-Bromo-2,4-dimethoxybenzaldehydeHCID 668346—
촉매HCID 178418397HCID 178418397—
용매1,2-DimethoxyethaneHCID 8071—
생성물5-Benzo[b]thiophen-2-yl-2,4-dimethoxy-benzaldehydeHCID 1611591683%

반응 단계

Ex-3A: A sample of 5-bromo-2,4-dimethoxybenzaldehyde (4.9 g, 20.0 mmol) was dissolved in ethylene glycol dimethyl ether (50 mL). Tetrakis(triphenylphosphine)palladium(0) (2.32 g, 2 mmol) was added, and the mixture was stirred at room temperature under nitrogen for 5 min. Benzo[b]thiophene-2-boronic acid (4.27 g, 24 mmol) and sodium carbonate solution (2 M, 20 mL) were added. The mixture was stirred at reflux under nitrogen for 24 hours. Upon cooling to room temperature, the mixture was poured into water and extracted with ethyl acetate. The organic phase was dried over sodium sulfate and evaporated. Silica gel chromatography (hexane/ethyl acetate 2:1 then 1:1) gave 4.75 g (83%) of the desired 5-(benzo[b]thien-2-yl)-2,4-dimethoxybenzaldehyde. 1H NMR (CDCl3) δ 10.36 (s, 1H), 8.20 (s, 1H), 7.83–7.78 (m, 2H), 7.68 (s, 1H), 7.36–7.27 (m, 2H), 6.54 (s, 1H), 4.06 (s, 3H), 4.00 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094801B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-c0e35e5b2743478c94c3b16684e200e4
출처 메모uspto-grants-2006_08