HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1293608Generated: October 29, 2026
2-Bromo-3-pyridinol → 2-Bromo-3-pyridyl trifluoromethanesulfonate
https://huagongshe.com/reaction/1293608
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Bromo-3-pyridinol | HCID 23070 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-Bromo-3-pyridyl trifluoromethanesulfonate | HCID 10686062 | 94% |
Reaction Steps
To a solution of 2-bromo-3-hydroxypyridine[CAS 6602–32–0, commercially available] (25.0 g, 144 mmol) in anhydrous pyridine (145 mL) at −10° C. (ice/NaCl) was drop wise added Tf2O (24.2 mL, 147 mmol) keeping the temperature below −5° C. (30 min). The cooling bath was removed and mixture was allowed to reach 23° C., stirred at 23° C. for 75 min, poured into sat. NaHCO3-sol., extracted with DCM, washed with brine, dried over Na2SO4. Removal of the solvent in vacuum left a brown oil, which was purified by vacuum distillation: bp 65° C. (0.82 mbar) (42 g colorless oil, with some solid); triturated with hexane, filtered the undesired solid off, washed with hexane, collected the mother liquor, evaporated the solvent to give the title compound as a colorless liquid (41.52 g, 94%). MS (TOF ESP) 306 [(M+H)+], 307.85 [(M+2+H)+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07238808B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-1b81cdbd25d544cdbab9060772edf080 |
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| Source note | uspto-grants-2007_07 |
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