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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713586Generated: October 26, 2026

Trifluoromethanesulfonic acid → HCID 117606250, compound

https://huagongshe.com/reaction/713586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic acidHCID 62406—
Reactant4-Methyl-N-(4-methylphenyl)-N-phenylbenzenamineHCID 88539—
Reactant10,11-diphenyl-11H-indeno[1,2-b]quinolin-11-olHCID 117606248—
SolventDichloromethaneHCID 6344—
ProductHCID 117606250HCID 11760625089.7%

Reaction Steps

In an embodiment, the starting material 10,11-diphenyl-11H-indeno[1,2-b]quinolin-11-ol (385 mg, 1.00 mmol) and 4-methyl-N-phenyl-N-(p-tolyl)aniline (328 mg, 1.20 mmol) are placed in a round bottom flask and then dissolved in 10 ml of dichloromethane. Subsequently, trifluoromethanesulfonic acid (0.13 ml, 1.50 mmol) is slowly dripped into the flask to promote reaction. After 12 hours of reaction at 140° C., the crude product is extracted with 50 ml of Ethyl acetate 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 575 mg of 4-(10,11-diphenyl-11H-indeno[1,2-b]quinolin-11-yl)-N,N-di-p-tolylaniline. The percentage yield is 89.7%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09184396B2
Source datasetuspto-grants-2015_11
ORD IDord-d3868a49f74e4e87aeceff3a52c8df37
Source noteuspto-grants-2015_11