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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10620생성일: 2026년 10월 24일

4-Acetylbenzoic Acid → 4-[3-(5-benzo[b]thiophen-2-yl-2,4-dimethoxy-phenyl)-E-acryloyl]-benzoic acid

https://huagongshe.com/ko/reaction/10620

반응식

참여 물질

역할이름HCID투입량
반응물4-Acetylbenzoic AcidHCID 11470—
반응물Sodium HydroxideHCID 14798—
반응물5-Benzo[b]thiophen-2-yl-2,4-dimethoxy-benzaldehydeHCID 16115916—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물4-[3-(5-benzo[b]thiophen-2-yl-2,4-dimethoxy-phenyl)-E-acryloyl]-benzoic acidHCID 993315054%

반응 단계

To a solution of 4-acetylbenzoic acid (1.50 g, 9.1 mmol) and 5-(benzo[b]thien-2-yl)-2,4-dimethoxybenzaldehyde from Ex-3A (3.27 g, 11.0 mmol) in N,N-dimethylformamide (76 mL) was added a solution of sodium hydroxide (5 M, 7.3 mL, 36.5 mmol). The reaction mixture was allowed to stir at room temperature for 2 h and was then diluted with water to a volume of 150 mL. The solution was washed with dichloromethane and acidified with concentrated sulfuric acid to pH=3. The resulting solution was then extracted with dichloromethane. The dichloromethane extract was washed with brine, dried over sodium sulfate and concentrated. The resulting oily product solidified in ethanol. The solid was further stirred in ethanol for one day and collected by filtration. The solid was washed with ethanol, then dried in vacuo to afford the title compound as a yellow solid (2.2 g, 54%). 1H NMR (300 MHz, DMSO-d6) δ 8.36 (s, 1H), 8.21 (d, 2H), 8.07 (m, 3H), 7.93 (m, 3H), 7.82 (d, 1H), 7.32 (m, 2H), 6.86 (s, 1H), 4.08 (s, 3H), 4.00 (s, 3H). Anal. Calculated for C26H20O5S·1/6H2O: C, 69.78; H, 4.58; S, 7.17; found: C, 69.95; H, 4.69; S, 7.15. HPLC purity: 97.9% (area percentage).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094801B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-80ec1d096bde430b80ffb02cef23687a
출처 메모uspto-grants-2006_08