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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1666791생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1666791

반응식

참여 물질

역할이름HCID투입량
반응물1,10-PhenanthrolineHCID 1318—
반응물Cesium carbonateHCID 10796—
반응물IodobenzeneHCID 11575—
반응물1H-Indole-6-carboxaldehydeHCID 2773435—
반응물trans-DibenzylideneacetoneHCID 5354370—
용매DichloromethaneHCID 6344—
용매O-XyleneHCID 7237—
용매Ammonium ChlorideHCID 25517—
생성물1-Phenyl-1H-indole-6-carbaldehydeHCID 21071394—

반응 조건

온도110 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08044090B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-8c35c81f2248442d9041f4460566c6d8
출처 메모uspto-grants-2011_10