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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713585Generated: October 26, 2026

9-(p-Tolyl)carbazole → 10,11-diphenyl-11-(9-(p-tolyl)-9H-carbazol-3-yl)-11H-indeno[1,2-b]quinoline

https://huagongshe.com/reaction/713585

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-(p-Tolyl)carbazoleHCID 15798651—
ReactantPhosphorus Pentoxide-Methanesulfonic AcidHCID 86584057—
Reactant10,11-diphenyl-11H-indeno[1,2-b]quinolin-11-olHCID 117606248—
SolventDichloromethaneHCID 6344—
Product10,11-diphenyl-11-(9-(p-tolyl)-9H-carbazol-3-yl)-11H-indeno[1,2-b]quinolineHCID 11760624683.4%

Reaction Steps

Referring to the reaction formula above, 10,11-diphenyl-11H-indeno[1,2-b]quinolin-11-ol (385 mg, 1.00 mmol) and 9-(p-tolyl)-9H-carbazole (291 mg, 1.20 mmol) are placed in a round bottom flask and then dissolved in 5 ml of dichloromethane. Subsequently, 286 of Eaton's reagent is slowly dripped into the flask to promote reaction. After 12 hours of reaction at 100° C., the crude product is extracted with 8 ml of dichloromethane and sodium bicarbonate for three times. Finally, an organic layer of the crude product is dehydrated with magnesium sulfate and concentrated to be sublimated and purified to obtain 521 mg of 10,11-diphenyl-11-(9-(p-tolyl)-9H-carbazol-3-yl)-11H-indeno[1,2-b]quinoline. The percentage yield is 83.4%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09184396B2
Source datasetuspto-grants-2015_11
ORD IDord-ede88c5e066940a39e26a56ea8189a46
Source noteuspto-grants-2015_11