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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467418Generated: October 29, 2026

2,6-Lutidine → Triphenylenyl trifluoromethanesulfonate

https://huagongshe.com/reaction/467418

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantTriphenylen-2-olHCID 3016112—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductTriphenylenyl trifluoromethanesulfonateHCID 8664772490%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623520B2
Source datasetuspto-grants-2014_01
ORD IDord-f83cdeeb17f941808b7427d4f2f47738
Source noteuspto-grants-2014_01