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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 446062생성일: 2026년 10월 26일

Water → 5-(3-Bromophenyl)-2-furaldehyde

https://huagongshe.com/reaction/446062

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium CarbonateHCID 10340—
반응물Benzene, 1-bromo-3-iodo-HCID 11561—
반응물5-Formylfuran-2-boronic acidHCID 2734355—
촉매HCID 178418397HCID 178418397—
용매1,2-DimethoxyethaneHCID 8071—
생성물5-(3-Bromophenyl)-2-furaldehydeHCID 84051725.9%

반응 단계

5-Formyl-2-furanboronic acid (676 mg, 4.8 mmol) and 3-bromoiodobenzene (1132 mg, 4 mmol) were dissolved in 1,2-dimethoxyethane (30 mL), tetrakis(triphenylphosphine)palladium (228 mg, 0.2 mmol) was added thereto, 2 mol/L sodium carbonate (9.6 mL) was further added thereto, and the mixture was heated to reflux for 2 hours while stirring. After the reaction was completed water (20 mL) was added thereto, and extraction with ethyl acetate (20 mL×2) was carried out. The organic layer was washed with saturated brine, water was removed using anhydrous sodium sulfate, the solvent was then removed by evaporation under reduced pressure, and the residue was subjected to silica gel column chromatography using ethyl acetate/hexane (3/7 (volume ratio)) as an eluent, to give 5-(3-bromophenyl)furan-2-carbaldehyde in a yield of 306 mg (yield 25.9%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08476449B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-5e7c749d4a9446d4a9a263f8c69dd32d
출처 메모uspto-grants-2013_07