Sodium borohydride → (5-Fluoropyridin-2-yl)methanol

HRID 79474Notes

Reaction equation

HRID 79474 reaction equation
[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]=[O:9])=[N:6][CH:7]=1.[BH4-].[Na+]>CO>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][OH:9])=[N:6][CH:7]=1

Participants

4

Procedure

A suspension of 5-fluoropicolinaldehyde (10.0 g, 79.94 mmol) in MeOH (160 mL) was treated with sodium borohydride (9.073 g, 239.8 mmol) in portions. The mixture was stirred at ambient temperature for 16 hours. The mixture was quenched with water, concentrated under reduced pressure, diluted with water and extracted with EtOAc. The combined organic extracts were dried (phase separator silicone treated filter paper), and concentrated under reduced pressure to give a clear oil, which was triturated with ether. The resulting solid was collected by filtration to afford (5-fluoropyridin-2-yl)methanol (10.15 g, 99% yield).

Workup

  1. customThe mixture was quenched with water
  2. concentrationconcentrated under reduced pressure
  3. additiondiluted with water
  4. extractionextracted with EtOAc
  5. customThe combined organic extracts were dried
  6. addition(phase separator silicone treated filter paper)
  7. concentrationconcentrated under reduced pressure
  8. customto give a clear oil, which
  9. customwas triturated with ether
  10. filtrationThe resulting solid was collected by filtration

Sources & evidence

ORD record
ord-0ae13b38200f44a191d054b114a70d11
Source dataset
uspto-grants-2014_09
Patent number
US08841455B2

Reaction notes

Loading…