HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455355Generated: October 31, 2026
Potassium Phosphate, Tribasic → 2-Phenylisonicotinic acid
https://huagongshe.com/reaction/1455355
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | 2-Bromoisonicotinic acid | HCID 222701 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Phenylisonicotinic acid | HCID 2762845 | 53% |
Reaction Steps
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+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07482335B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-1ab012992eff460fb03e64846295ce61 |
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| Source note | uspto-grants-2009_01 |
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