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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1371848Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1371848

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,10-PhenanthrolineHCID 1318—
EduktCesium carbonateHCID 10796—
EduktIodobenzeneHCID 11575—
Edukt1H-Indole-6-carboxaldehydeHCID 2773435—
Edukttrans-DibenzylideneacetoneHCID 5354370—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelO-XyleneHCID 7237—
LösungsmittelAmmonium ChlorideHCID 25517—
Produkt1-Phenyl-1H-indole-6-carbaldehydeHCID 21071394—

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07157488B2
Quelldatensatzuspto-grants-2007_01
ORD IDord-463b9612b6b44288b2f7c6f4e2f531bb
Quellennotizuspto-grants-2007_01