HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713586Generated: October 26, 2026
Trifluoromethanesulfonic acid → HCID 117606250, compound
https://huagongshe.com/reaction/713586
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | 4-Methyl-N-(4-methylphenyl)-N-phenylbenzenamine | HCID 88539 | — |
| Reactant | 10,11-diphenyl-11H-indeno[1,2-b]quinolin-11-ol | HCID 117606248 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 117606250 | HCID 117606250 | 89.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09184396B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-d3868a49f74e4e87aeceff3a52c8df37 |
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| Source note | uspto-grants-2015_11 |
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