HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467418Generated: October 29, 2026
2,6-Lutidine → Triphenylenyl trifluoromethanesulfonate
https://huagongshe.com/reaction/467418
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | Triphenylen-2-ol | HCID 3016112 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Triphenylenyl trifluoromethanesulfonate | HCID 86647724 | 90% |
Reaction Steps
Under an argon atmosphere, 12.5 g of 2-hydroxytriphenylene and 0.93 g of 4-dimethylaminopiridine were placed in a flask, 200 mL of methylene chloride was added thereto and the reaction solution was cooled to −78° C. 8.22 g of 2,6-dimethylpiridine was added to the reaction solution and then, 17.3 g of trifluoromethanesulfonic acid anhydride was dropwise added thereto. The reaction solution was stirred for 5 hours while increasing temperature of the reaction solution to room temperature. The deposited solid was collected by filtration, washed with water and methanol and then dried to obtain 17.3 g (yield: 90%) of triphenylenyl trifluoromethanesulfonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08623520B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-f83cdeeb17f941808b7427d4f2f47738 |
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| Source note | uspto-grants-2014_01 |
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