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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455355Generated: October 31, 2026

Potassium Phosphate, Tribasic → 2-Phenylisonicotinic acid

https://huagongshe.com/reaction/1455355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantPhenylboronic AcidHCID 66827—
Reactant2-Bromoisonicotinic acidHCID 222701—
SolventDimethylformamideHCID 6228—
Product2-Phenylisonicotinic acidHCID 276284553%

Reaction Conditions

Temperature150 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482335B2
Source datasetuspto-grants-2009_01
ORD IDord-1ab012992eff460fb03e64846295ce61
Source noteuspto-grants-2009_01