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3-Hydroxybenzyl alcohol → 3-(Pyridin-2-yloxy)benzaldehyde

HRID 1678582
Notes
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Reaction equation

HRID 1678582 reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH2:5][OH:6].Br[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][N:12]=1.C(=O)([O-])[O-].[K+].[K+]>N1C=CC=CC=1>[N:12]1[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=1[O:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[O:6]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 1023-Hydroxybenzyl alcoholHCID 79732-BromopyridineHCID 11430Potassium Carbonate

Product 1

HCID 27353633-(Pyridin-2-yloxy)benzaldehydeYield 61%

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Conditions

Temperature
90 °C

Procedure

3-Hydroxybenzyl alcohol (1.0 g, 8.2 mmol) was dissolved in pyridine (20 mL). 2-Bromopyridine (1.6 g, 9.8 mmol) and potassium carbonate (2.3 g, 16.4 mmol) were added thereto, and then the mixture was stirred at 90° C. for 10 minutes. Copper oxide(II) (1.6 g, 20.5 mmol) was further added thereto, and the reaction mixture was heated under reflux for 2 days. The reaction solution was filtered, and concentrated under reduced pressure. To the residue was added water, and the mixture was extracted with ethyl acetate. The extract was dried, and then concentrated under reduced pressure. The residue was purified with silica gel column chromatography (hexane/ethyl acetate=100:0 to 70:30) to give the title compound (1.0 mg, yield 61%).

Workup

  1. temperaturethe reaction mixture was heated
  2. temperatureunder reflux for 2 days
  3. filtrationThe reaction solution was filtered
  4. concentrationconcentrated under reduced pressure
  5. additionTo the residue was added water
  6. extractionthe mixture was extracted with ethyl acetate
  7. customThe extract was dried
  8. concentrationconcentrated under reduced pressure
  9. customThe residue was purified with silica gel column chromatography (hexane/ethyl acetate=100:0 to 70:30)

Sources & evidence

ORD record
ord-6c30dd5c1b6f42d292cc86e16b1882fc
Source dataset
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08008525B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes