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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 332615생성일: 2026년 10월 26일

Acetic Acid → 4-Ethoxycarbonylfuran-2-carboxylic acid

https://huagongshe.com/reaction/332615

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Hydrochloric AcidHCID 313—
반응물WaterHCID 962—
반응물TriethylamineHCID 8471—
반응물TriphenylphosphineHCID 11776—
반응물BromineHCID 24408—
반응물Ethyl 3-furoateHCID 69201—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
생성물4-Ethoxycarbonylfuran-2-carboxylic acidHCID 53429231—

반응 단계

3-Furancarboxylic acid ethyl ester (1.4 g, 10.0 mmol) was dissolved in acetic acid (10 mL), bromine (1.6 g, 10.0 mmol) was added, and the mixture was stirred overnight. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=80/20). The obtained crude fraction was dissolved in N,N-dimethylformamide (15 mL), palladium acetate (0.18 g, 0.78 mmol), triphenylphosphine (0.41 g, 1.55 mmol), triethylamine (2.2 mL, 15.5 mmol), and water (0.7 mL, 38.8 mmol) were added, and the mixture was stirred at 80° C. overnight under a carbon monoxide atmosphere. 1N Hydrochloric acid was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was purified by high performance liquid chromatography to give the title compound (0.47 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08877805B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-5357d541ba694a70b16c8446760eac70
출처 메모uspto-grants-2014_11