Potassium Phosphate, Tribasic → 2-Phenylisonicotinic acid
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]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
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
- customPreparation H1, Step 1
- customwas degassed under vacuum/Ar
- additionA catalytic amount of tetrakis(triphenylphosphine)palladium(0) was added to the tube
- customthe mixture was degassed again
- customthe tube was sealed
- filtrationThe reaction mixture was filtered
- concentrationthe filtrate was concentrated in-vacuo
- dissolutionthe residue was dissolved in water (10 mL)
- additionThe mixture was acidified to pH=6 with the addition of 1.0 N HCl
- filtrationthe resulting precipitate was collected by filtration
- washrinsed with two portions of ice-cold water, and air
- customdried
Sources & evidence
- ORD record
- ord-1ab012992eff460fb03e64846295ce61
- Source dataset
- uspto-grants-2009_01
- Patent number
- US07482335B2
Reaction notes
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