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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207029Generated: November 1, 2026

Trifluoromethanesulfonic anhydride → 5-Bromo-2,7-dimethylquinolin-6-yl trifluoromethanesulfonate

https://huagongshe.com/reaction/2207029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant5-Bromo-2,7-dimethylquinolin-6-olHCID 66631416—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product5-Bromo-2,7-dimethylquinolin-6-yl trifluoromethanesulfonateHCID 86691977—

Reaction Steps

To a stirred solution of 5-bromo-2,7-dimethylquinolin-6-ol (1.04 g, 3.1 mmol) in dichloromethane (50 mL) and pyridine (10 mL) was added Tf2O (1.1 mL, 6.2 mmol) at 0° C. The mixture was stirred at room temperature for 2 hours, quenched with slowly addition of NaHCO3 solution at 0° C. The mixture was extracted with dichloromethane. The organic layer was washed with brine, dried and concentrated to give the desired product. Column purification gave pure product. LCMS-ESI+: calc'd for C12H9BrF3NO3S: 383.9 (M+H+); Found: 383.9 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376392B2
Source datasetuspto-grants-2016_06
ORD IDord-1eac5817ff6a4a2ebb63f3d760441755
Source noteuspto-grants-2016_06