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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1091311생성일: 2026년 10월 27일

Dimethylformamide → 3-Benzofurancarboxylic acid, methyl ester

https://huagongshe.com/reaction/1091311

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참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물TriethylamineHCID 8471—
반응물Benzo[b]furan-3-yl trifluoromethanesulfonateHCID 21480510—
촉매palladium(II) acetateHCID 167845—
촉매Bis(cyclopenta-2,4-dien-1-yl(phenyl)phosphane);iron(2+)HCID 133083342—
용매MethanolHCID 887—
생성물3-Benzofurancarboxylic acid, methyl esterHCID 1277709986%

반응 조건

온도60 °C

반응 단계

To a DMF (8.0 mL) solution of 1-benzofuran-3-yl trifluoromethanesulfonic acid (1.00 g, 3.76 mmol), 1,1′-diphenylphosphinoferrocene (128 mg, 231 μmol) and palladium acetate (26.0 mg, 116 μmol), methanol (3.5 mL) and triethylamine (1.05 mL, 7.53 mmol) were added thereto at room temperature. Carbon monoxide gas was bubbled for 20 minutes, and then under a carbon monoxide atmosphere, the mixture was heated and stirred at 60° C. for 3 hours. Water (50 mL) was added, and then the mixture was extracted with ethyl acetate (2×30 mL). The organic layer was combined, washed with 1N-hydrochloric acid (30 mL), and then dried over anhydrous magnesium sulfate. The solvent was concentrated under reduced pressure. The obtained residue was purified using silica gel flash column chromatography (Biotage AB: column No. 40M, hexane:diethyl ether=95:5), to obtain the title compound (570 mg, 3.24 mmol, 86%) as a transparent oily matter.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08129366B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-4307a233a64144fb982e361feb07303a
출처 메모uspto-grants-2012_03