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Carbonic acid sodium salt (1:2) → 5-(3-溴苯基)呋喃-2-甲醛
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)acetate | HCID 86675359 | — |
| 催化剂 | HCID 178418397 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 专利号 | US08476449B2 |
| 来源数据集 | uspto-grants-2013_07 |
| ORD ID | ord-53a0b689b8cf44aca1e2bf50b3017401 |
| 来源说明 | uspto-grants-2013_07 |