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HRID 1371848作成日:2026年10月25日

1,10-Phenanthroline → 1-Phenyl-1H-indole-6-carbaldehyde

https://huagongshe.com/reaction/1371848

反応式

関与物質

役割名称HCID仕込み量
反応物1,10-PhenanthrolineHCID 1318—
反応物Cesium carbonateHCID 10796—
反応物IodobenzeneHCID 11575—
反応物1H-Indole-6-carboxaldehydeHCID 2773435—
反応物trans-DibenzylideneacetoneHCID 5354370—
溶媒DichloromethaneHCID 6344—
溶媒O-XyleneHCID 7237—
溶媒Ammonium ChlorideHCID 25517—
生成物1-Phenyl-1H-indole-6-carbaldehydeHCID 21071394—

反応条件

温度110 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07157488B2
出典データセットuspto-grants-2007_01
ORD IDord-463b9612b6b44288b2f7c6f4e2f531bb
出典メモuspto-grants-2007_01