Potassium Phosphate, Tribasic → 2-Phenylisonicotinic acid

HRID 1455355Notes

Reaction equation

HRID 1455355 reaction equation
Br[C:2]1[CH:7]=[C:6]([C:8]([OH:10])=[O:9])[CH:5]=[CH:4][N:3]=1.[C:11]1(B(O)O)[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.P([O-])([O-])([O-])=O.[K+].[K+].[K+]>CN(C=O)C>[C:11]1([C:2]2[CH:7]=[C:6]([CH:5]=[CH:4][N:3]=2)[C:8]([OH:10])=[O:9])[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1

Participants

5

Conditions

Temperature
150 °C

Procedure

Preparation H1, Step 1: A mixture of 2-bromo-4-pyridinecarboxylic acid (1.1 g, 5.45 mmol), phenylboronic acid (1.3 g, 10.9 mmol), 2.0 M potassium phosphate (aq) (8.2 mL, 16.34 mmol), and DMF (10 mL) in a 20 mL microwave tube was degassed under vacuum/Ar. A catalytic amount of tetrakis(triphenylphosphine)palladium(0) was added to the tube, the mixture was degassed again, the tube was sealed, and the reaction was heated at 150° C. in the microwave for 30 min. The reaction mixture was filtered, the filtrate was concentrated in-vacuo, and the residue was dissolved in water (10 mL). The mixture was acidified to pH=6 with the addition of 1.0 N HCl, and the resulting precipitate was collected by filtration, rinsed with two portions of ice-cold water, and air dried to yield 575 mg of 2-phenylisonicotinic acid as an off-white solid. MS (ES+)=200 (M+H+).

Workup

  1. customPreparation H1, Step 1
  2. customwas degassed under vacuum/Ar
  3. additionA catalytic amount of tetrakis(triphenylphosphine)palladium(0) was added to the tube
  4. customthe mixture was degassed again
  5. customthe tube was sealed
  6. filtrationThe reaction mixture was filtered
  7. concentrationthe filtrate was concentrated in-vacuo
  8. dissolutionthe residue was dissolved in water (10 mL)
  9. additionThe mixture was acidified to pH=6 with the addition of 1.0 N HCl
  10. filtrationthe resulting precipitate was collected by filtration
  11. washrinsed with two portions of ice-cold water, and air
  12. customdried

Sources & evidence

ORD record
ord-1ab012992eff460fb03e64846295ce61
Source dataset
uspto-grants-2009_01
Patent number
US07482335B2

Reaction notes

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