Water → 4-Pyridin-3-yl-benzoic acid

HRID 1242552Notes

Reaction equation

HRID 1242552 reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C:7]2[CH:12]=[CH:11][C:10]([CH3:13])=[CH:9][CH:8]=2)[CH:2]=1.[O-:14][Mn](=O)(=O)=O.[K+].[OH2:20]>N1C=CC=CC=1>[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C:7]2[CH:8]=[CH:9][C:10]([C:13]([OH:14])=[O:20])=[CH:11][CH:12]=2)[CH:2]=1

Participants

5

Reactant 3

HCID 962WaterHCID 516875Potassium PermanganateHCID 41331893-(4-methylphenyl)pyridine

Product 1

HCID 15152444-Pyridin-3-yl-benzoic acidYield 76%

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Procedure

To a mixture of 4-(3-pyridyl)toluene (35 g, 0.207 mol) in pyridine (400 ml) and water (400 ml) was added KMnO4 (163 g, 1.03 mol) in portions and refluxed for 12 h. The reaction mixture was filtered through celite and acidified with conc. HCl. The product was washed with water and dried to give 4-(3-pyridyl)benzoic acid (32 g, 76%) as a white solid. To a mixture of 4-(3-pyridyl)benzoic acid (22 g, 0.11 mol) in THF (2.51), mCPBA (152 g, 0.44 mol, 50%) was added and stirred at RT for 12 h. The solid was filtered, and washed with THF to give 4-(1-oxido-3-pyridinyl)benzoic acid (20 g, 86%).

Workup

  1. temperaturerefluxed for 12 h
  2. filtrationThe reaction mixture was filtered through celite
  3. washThe product was washed with water
  4. customdried

Sources & evidence

ORD record
ord-c803635a55ee4dffbe006542112a5b51
Source dataset
uspto-grants-2006_10
Patent number
US07115639B2

Reaction notes

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