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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207041Generated: November 1, 2026

Trifluoromethanesulfonic anhydride → 5-Bromo-7-methylquinolin-6-yl trifluoromethanesulfonate

https://huagongshe.com/reaction/2207041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant5-Bromo-6-hydroxy-7-methyl-quinolineHCID 23078309—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product5-Bromo-7-methylquinolin-6-yl trifluoromethanesulfonateHCID 86691979—

Reaction Conditions

Temperature0 °C

Reaction Steps

To the solution of 5-bromo-7-methylquinolin-6-ol (238 mg, 1.0 mmol) in dichloromethane (10 mL) and pyridine (2 mL) was added Tf2O (0.34 mL, 2.0 mmol) at −30° C. The mixture was stirred and warmed to 0° C. over a period of 2 hours. The reaction was quenched with slow addition of NaHCO3 solution. The mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate and concentrated to give 5-bromo-7-methylquinolin-6-yl trifluoromethanesulfonate. LCMS-ESI+ (m/z): 369.9, 371.9 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376392B2
Source datasetuspto-grants-2016_06
ORD IDord-a5b88ba689c94fda8115f60553302011
Source noteuspto-grants-2016_06