5-Bromopyridine-2-carboxylic acid → (5-Bromopyridin-2-yl)methanol

HRID 467615Notes

Reaction equation

HRID 467615 reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:8](O)=[O:9])=[N:6][CH:7]=1.B.CSC>C1COCC1>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][OH:9])=[N:6][CH:7]=1

Participants

4

Procedure

To a solution of 5-bromopyridin-2-carboxylic acid (8 g, 42.1 mmol) in THF (100 ml) was added borane-dimethylsulphide (16 ml, 168.30 mmol) dropwise at 0° C. After warming-up to ambient temperature stirring was continued for 24 hours. The solution was cooled again to 0° C., quenched with MeOH and refluxed for 1 h. Solvents were removed and the residue was treated with water. The aqueous phase was extracted with ethyl acetate and the combined organic layers were washed with water and brine, dried, filtered and concentrated under reduced pressure to afford 4.76 g (64%) of the title compound.

Workup

  1. temperatureThe solution was cooled again to 0° C.
  2. customquenched with MeOH
  3. temperaturerefluxed for 1 h
  4. customSolvents were removed
  5. additionthe residue was treated with water
  6. extractionThe aqueous phase was extracted with ethyl acetate
  7. washthe combined organic layers were washed with water and brine
  8. customdried
  9. filtrationfiltered
  10. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-cf68c54a4eb34ea8a9f9a9e43ddeff7a
Source dataset
uspto-grants-2014_01
Patent number
US08623866B2

Reaction notes

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