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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 446054생성일: 2026년 10월 27일

Sodium Carbonate → 5-(3-Bromophenyl)-2-furaldehyde

https://huagongshe.com/reaction/446054

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물Benzene, 1-bromo-3-iodo-HCID 11561—
반응물5-Formylfuran-2-boronic acidHCID 2734355—
반응물(Z)-ethyl-2-(5-oxo-2-thioxo-4-((5-(3-(tributylstannyl)phenyl)furan-2-yl)methylene)imidazolidin-1-yl)acetateHCID 86675359—
촉매HCID 178418397HCID 178418397—
용매1,2-DimethoxyethaneHCID 8071—
생성물5-(3-Bromophenyl)-2-furaldehydeHCID 840517—

반응 단계

Synthesis of (Z)-ethyl-2-(5-oxo-2-thioxo-4-((5-(3-(tributylstannyl)phenyl)furan-2-yl)methylene)imidazolidin-1-yl)acetate may be carried out in accordance with a known method, for example, a method described in non-patent document 2. First, substantially equivalent amounts of 5-formyl-2-furanboronic acid and 3-bromoiodobenzene are dissolved in 1,2-dimethoxyethane, and sodium carbonate and a catalytic amount of tetrakis(triphenylphosphine)palladium are added thereto. This solution is heated to reflux while stirring so as to carry out a reaction. After the reaction is complete, the solvent is removed by evaporation. Then, purification is carried out to give 5-(3-bromophenyl)furan-2-carbaldehyde (FIG. 1, step 1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08476449B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-53a0b689b8cf44aca1e2bf50b3017401
출처 메모uspto-grants-2013_07