2-Bromo-3-pyridinol → 2-Bromo-3-pyridyl trifluoromethanesulfonate

HRID 558497Notes

Reaction equation

HRID 558497 reaction equation
[Br:1][C:2]1[C:7]([OH:8])=[CH:6][CH:5]=[CH:4][N:3]=1.[O:9](S(C(F)(F)F)(=O)=O)[S:10]([C:13]([F:16])([F:15])[F:14])(=O)=[O:11]>N1C=CC=CC=1>[Br:1][C:2]1[C:7]([O:8][S:10]([C:13]([F:16])([F:15])[F:14])(=[O:11])=[O:9])=[CH:6][CH:5]=[CH:4][N:3]=1

Participants

4

Conditions

Temperature
23 °C

Procedure

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)+].

Workup

  1. customat −10° C.
  2. customthe temperature below −5° C. (30 min)
  3. customThe cooling bath was removed
  4. customto reach 23° C.
  5. additionpoured into sat. NaHCO3-sol
  6. extraction, extracted with DCM
  7. washwashed with brine
  8. dry with materialdried over Na2SO4
  9. customRemoval of the solvent in vacuum
  10. waitleft a brown oil, which
  11. distillationwas purified by vacuum distillation
  12. customtriturated with hexane
  13. filtrationfiltered the undesired solid off,
  14. washwashed with hexane
  15. customcollected the mother liquor
  16. customevaporated the solvent

Sources & evidence

ORD record
ord-f50f3a78940e4ad98a942d32ddfa4d8e
Source dataset
uspto-grants-2011_11
Patent number
US08063048B2

Reaction notes

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