참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,10-Phenanthroline | HCID 1318 | — |
| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | Iodobenzene | HCID 11575 | — |
| 반응물 | 1H-Indole-6-carboxaldehyde | HCID 2773435 | — |
| 반응물 | trans-Dibenzylideneacetone | HCID 5354370 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | O-Xylene | HCID 7237 | — |
| 용매 | Ammonium Chloride | HCID 25517 | — |
| 생성물 | 1-Phenyl-1H-indole-6-carbaldehyde | HCID 21071394 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07157488B2 |
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| 출처 데이터셋 | uspto-grants-2007_01 |
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| ORD ID | ord-463b9612b6b44288b2f7c6f4e2f531bb |
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| 출처 메모 | uspto-grants-2007_01 |
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