HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207018Generated: October 31, 2026
Trifluoromethanesulfonic anhydride → 5-Bromo-7-methylquinolin-6-yl trifluoromethanesulfonate
https://huagongshe.com/reaction/2207018
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | 5-Bromo-6-hydroxy-7-methyl-quinoline | HCID 23078309 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Bromo-7-methylquinolin-6-yl trifluoromethanesulfonate | HCID 86691979 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376392B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-cb286cb5921547198c42f5c01b3f6e90 |
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| Source note | uspto-grants-2016_06 |
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