Bromine → HCID 178517592, compound

HRID 517971

Reaction equation

HRID 517971 reaction equation
[OH:1][C:2]1[C:7]([C:8]([F:11])([F:10])[F:9])=[CH:6][CH:5]=[CH:4][N:3]=1.[Br:12]Br>CO>[Br:12][C:5]1[CH:6]=[C:7]([C:8]([F:9])([F:11])[F:10])[C:2]([OH:1])=[N:3][CH:4]=1

Participants

4

Procedure

A solution of 2-hydroxy-3-(trifluoromethyl)pyridine (10.0 g) and bromine (3.08 ml, 9.60 g) in methanol (50 ml) was stirred at 20° C. for 22 h. The solution was concentrated and the residue partitioned between ethyl acetate (400 ml) and water (100 ml). The layers were separated and the organic layer was washed with 5% Na2S2O3aq. (100 ml) and brine (100 ml), dried over sodium sulphate, filtered and concentrated. Purified by Biotage SNAP cartridge KP-Sil column twice (100 g, heptane:ethyl acetate=1:0, 3:1 to 2:1) to give 13.69 g light yellow solid as 5-bromo-2-hydroxy-3-(trifluoromethyl)pyridine (95%).

Workup

  1. concentrationThe solution was concentrated
  2. customthe residue partitioned between ethyl acetate (400 ml) and water (100 ml)
  3. customThe layers were separated
  4. washthe organic layer was washed with 5% Na2S2O3aq
  5. dry with material(100 ml) and brine (100 ml), dried over sodium sulphate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customPurified by Biotage SNAP cartridge KP-Sil column twice (100 g, heptane:ethyl acetate=1:0, 3:1 to 2:1)

Sources & evidence

ORD record
ord-a9b9b295723d4dd89022c3f180cfbf97
Source dataset
uspto-grants-2015_08
Patent number
US09115126B2

Linked notes

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