返回
化工社化工社化学信息打印报告 · 仅供科研参考
HRID 446054生成日期:2026年10月23日

Carbonic acid sodium salt (1:2) → 5-(3-溴苯基)呋喃-2-甲醛

https://huagongshe.com/zh-CN/reaction/446054

反应方程式

参与物

角色名称HCID投料
反应物Carbonic acid sodium salt (1:2)HCID 10340—
反应物1-溴-3-碘苯HCID 11561—
反应物5-甲醛基呋喃-2-硼酸HCID 2734355—
反应物(Z)-ethyl-2-(5-oxo-2-thioxo-4-((5-(3-(tributylstannyl)phenyl)furan-2-yl)methylene)imidazolidin-1-yl)acetateHCID 86675359—
催化剂HCID 178418397HCID 178418397—
溶剂乙二醇二甲醚HCID 8071—
产物5-(3-溴苯基)呋喃-2-甲醛HCID 840517—

反应步骤

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).

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US08476449B2
来源数据集uspto-grants-2013_07
ORD IDord-53a0b689b8cf44aca1e2bf50b3017401
来源说明uspto-grants-2013_07