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3-Pyrid-2-ylbenzoic acid

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Company Name: Nanjing Chemlin Chemical Co., Ltd  
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3-Pyrid-2-ylbenzoic acid manufacturers

3-Pyrid-2-ylbenzoic acid Basic information
Product Name:3-Pyrid-2-ylbenzoic acid
Synonyms:3-(2-pyridinyl)benzoate;3-Pyridin-2-yl-benzoic acid 97%;3-(2-PYRIDINYL)BENZOIC ACID;AKOS BAR-0487;3-PYRIDIN-2-YL-BENZOIC ACID;2-Pyridyl-3-benzoic acid;Benzoic acid, 3-(2-pyridinyl)-;3-Pyridin-2-ylbenzoate
CAS:4467-07-6
MF:C12H9NO2
MW:199.21
EINECS:
Product Categories:API intermediates
Mol File:4467-07-6.mol
3-Pyrid-2-ylbenzoic acid Structure
3-Pyrid-2-ylbenzoic acid Chemical Properties
Melting point 207 °C
Boiling point 409.0±28.0 °C(Predicted)
density 1.241±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
form solid
pka3.49±0.10(Predicted)
color Off-white
Safety Information
Hazard Codes Xn
Risk Statements 22
HS Code 2933399990
MSDS Information
3-Pyrid-2-ylbenzoic acid Usage And Synthesis
Synthesis
2-Bromopyridine

109-04-6

3-Carboxyphenylboronic acid

25487-66-5

3-PYRID-2-YLBENZOIC ACID

4467-07-6

General procedure for the synthesis of 3-(2-pyridyl)benzoic acid from 2-bromopyridine and 3-carboxyphenylboronic acid: to a mixed solution of acetonitrile (40 mL) and water (40 mL) containing 3-carboxyphenylboronic acid (1.66 g, 10 mmol) and 2-bromopyridine (1.72 g, 11 mmol), potassium carbonate (5.5 g, 40 mmol) and bis(triphenylphosphine) palladium(II) chloride (400 mg, 0.37 mmol). The reaction mixture was degassed and displaced three times with nitrogen. Subsequently, the mixture was stirred and reacted at 100 °C for 24 hours. After completion of the reaction, the reaction suspension was filtered while hot and the filtrate was concentrated to half of the original volume. The concentrated aqueous phase was washed with dichloromethane, and then the pH of the aqueous phase was adjusted to 3 with 1 M hydrochloric acid.The precipitated solid was collected by filtration, washed with water, and finally dried under vacuum to give 1.69 g of the white solid product 3-(2-pyridyl)benzoic acid in 85% yield. The product was detected by LC-MS (ESI), m/z: 200 (M + 1)+.

References[1] Patent: US2009/197863, 2009, A1. Location in patent: Page/Page column 75
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