関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1,10-Phenanthroline | HCID 1318 | — |
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | Iodobenzene | HCID 11575 | — |
| 反応物 | 1H-Indole-6-carboxaldehyde | HCID 2773435 | — |
| 反応物 | trans-Dibenzylideneacetone | HCID 5354370 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | O-Xylene | HCID 7237 | — |
| 溶媒 | Ammonium Chloride | HCID 25517 | — |
| 生成物 | 1-Phenyl-1H-indole-6-carbaldehyde | HCID 21071394 | — |
反応手順
Combine in a sealed tube 1H-indole-6-carbaldehyde 0.9 g, 6.2 mmol), copper(I) trifluoromethanesulfate—complex (0.2 g, 0.3 mmol), phenanthroline (1.3 g, 6.2 mmol), transdibenzylidenacetone (0.1 g, 0.3 mmol), cesium carbonate (2.6 g, 7.9 mmol) and iodobenzene (1.6 ml, 14.3 mmol) in xylene (40 ml). Heat at about 110° C. After 24 hours, cool to room temperature, dilute with dichloromethane and saturated ammonium chloride. Separate the layer and Extract the aqueous layer with dichloromethane. Combine the organic layers and wash sequentially with distilled water and brine and then dry (Na2SO4), filter, and concentrated to give a residue. Chromatograph the residue eluting with 8:2 hexane:EtOAc to give the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07157488B2 |
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| 出典データセット | uspto-grants-2007_01 |
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| ORD ID | ord-463b9612b6b44288b2f7c6f4e2f531bb |
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| 出典メモ | uspto-grants-2007_01 |
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