Dimethylformamide → 3-Fluoro-4-(pyridin-2-ylmethoxy)-benzaldehyde

HRID 1891770Notes

Reaction equation

HRID 1891770 reaction equation
CN(C)C=O.[OH:6][CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][N:9]=1.[H-].[Na+].[F:16][C:17]1[CH:18]=[C:19]([CH:22]=[CH:23][C:24]=1F)[CH:20]=[O:21]>O>[F:16][C:17]1[CH:18]=[C:19]([CH:22]=[CH:23][C:24]=1[O:6][CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][N:9]=1)[CH:20]=[O:21]

Participants

6

Reactant 4

HCID 6228DimethylformamideHCID 11474PiconolHCID 24758Sodium hydrideHCID 5880883,4-Difluorobenzaldehyde

Product 1

HCID 592552243-Fluoro-4-(pyridin-2-ylmethoxy)-benzaldehydeYield 45.6%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

To an N,N-dimethylformamide (40.0 mL) solution of 2-(hydroxymethyl)-pyridine (3.00 g, 27.5 mmol) was added sodium hydride (1.00 g, 25.0 mmol, 60% in oil) under nitrogen atmosphere at 0° C., which was stirred for 20 minutes at room temperature. 3,4-Difluorobenzaldehyde (4.69 g, 33.0 mmol) was then added at 0° C., and stirred for 20 minutes at room temperature. Water was added to the reaction solution at room temperature, which was then extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, and the solvent was evaporated under a reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:heptane=1:1→2:1) to obtain the title compound (2.90 g, 45.6%).

Workup

  1. stirringstirred for 20 minutes at room temperature
  2. extractionwhich was then extracted with ethyl acetate
  3. washThe organic layer was washed with saturated aqueous sodium chloride
  4. customthe solvent was evaporated under a reduced pressure
  5. customThe residue was purified by silica gel column chromatography (ethyl acetate:heptane=1:1→2:1)

Sources & evidence

ORD record
ord-6f5f90d692ef4684a727a8185439dfd6
Source dataset
uspto-grants-2013_08
Patent number
US08507530B2

Reaction notes

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