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HRID 27003Erstellt: 24. Oktober 2026

4,4'-Bis(dimethylamino)benzophenone → 6,6-Bis(p-dimethylaminophenyl)-6,11-dihydro-[1]benzopyrano[4,3-b]indole

https://huagongshe.com/de/reaction/27003

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4,4'-Bis(dimethylamino)benzophenoneHCID 7031—
EduktSodium HydroxideHCID 14798—
EduktPhosphorus oxychlorideHCID 24813—
Edukt2-(1H-indol-2-yl)phenolHCID 700009—
LösungsmittelChloroformHCID 6212—
Produkt6,6-Bis(p-dimethylaminophenyl)-6,11-dihydro-[1]benzopyrano[4,3-b]indoleHCID 1263269130,4%

Reaktionsschritte

7.7 g of 4,4'-bisdimethylaminobenzophenone was dissolved in 50 ml of chloroform, and the solution was stirred. Phosphorus oxychloride (5 g) and 10 ml of chloroform were added thereto, and the mixture was stirred for 30 minutes at room temperature (about 20°-30° C.). Then, 6 g of 2-(2'-hydroxyphenyl)indole was added thereto, and the mixture was stirred at room temperature for 3 hours. The mixture was heated under reflux for an additional 2 hours. The heated mixture was cooled to room temperature, and poured into ice water, and neutralized with an aqueous solution of sodium hydroxide. Furthermore, 200 to 300 ml of chloroform was added for extraction. The chloroform layer was washed with water, dried, and distilled under reduced pressure to remove the chloroform. The remaining oily substance was dissolved in a small amount of methanol by heating, and the solution was cooled. The crystals precipitated were separated by filtration, and dried to obtain 4 g of the objective compound having a melting point of 165° to 168° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04220356
Quelldatensatzuspto-grants-1980_09
ORD IDord-f245225b407842029f8a857b573e11cc
Quellennotizuspto-grants-1980_09