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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10629생성일: 2026년 10월 25일

4-Acetylbenzoic Acid → 4-[3E-(4-Pyrrolidin-1-yl-3-thiophen-2-yl-phenyl)-acryloyl]-benzoic acid

https://huagongshe.com/reaction/10629

반응식

참여 물질

역할이름HCID투입량
반응물4-Acetylbenzoic AcidHCID 11470—
반응물Sodium HydroxideHCID 14798—
반응물4-Pyrrolidin-1-yl-3-(thiophen-2-yl)-benzaldehydeHCID 21981055—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물4-[3E-(4-Pyrrolidin-1-yl-3-thiophen-2-yl-phenyl)-acryloyl]-benzoic acidHCID 2104162513%

반응 단계

4-Pyrrolidin-1-yl-3-(thiophen-2-yl)-benzaldehyde (400 mg, 1.55 mmol) from Ex-20B and 4-acetylbenzoic acid (255 mg, 1.55 mmol) were dissolved in dimethylformamide (30 mL). Sodium hydroxide solution (5 N, 1.25 mL) was added in one portion, and the mixture was stirred at room temperature overnight. The reaction was diluted with water (100 mL) and washed with ethyl acetate (100 mL). The aqueous phase was acidified with conc. HCl and extracted with ethyl acetate (2×100 mL). The organic phase was dried over magnesium sulfate and concentrated under reduced pressure. Silica gel chromatography (100% ethyl acetate) followed by recrystallization from ethanol provided 80 mg (13%) of the title compound as a solid, m.p. 212–214° C. with decomposition. 1H-NMR (300 MHz, CDCl3) δ 8.21 (d, 2H, J=8.4 Hz), 7.06 (d, 2H, J=8.4 Hz), 7.80 (d, 1H, J=15.3 Hz), 7.58 (d, 1H, J=1.9 Hz), 7.52 (dd, 1H, J=8.5 and 1.9 Hz), 7.33 (m, 1H), 7.32 (d, 1H, 15.3 Hz), 7.01–7.06 (m, 2H), 6.82 (d, 1H, 7.9 Hz), 3.12 (m, 4H), 1.84 (m, 4H). MS m/z=403 ([M]+, 100%). HRMS (EI) Calcd. for C24H21NO3S: 403.1242. Found: 403.1251.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094801B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-3710f1d466844c3a80b01c2a0dd8ec27
출처 메모uspto-grants-2006_08