2,2'-BIPYRIDINE-5-CARBOXYLIC ACID

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Products Intro: Product Name:2,2'-Bipyridine-5-carboxylic acid
CAS:1970-80-5
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Products Intro: Product Name:,2'-BIPYRIDINE-5-CARBOXYLIC ACID
CAS:1970-80-5
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Products Intro: Product Name:6-pyridin-2-ylpyridine-3-carboxylic acid
CAS:1970-80-5
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Products Intro: Product Name:5-Carboxy-2,2’-bipyridine
CAS:1970-80-5
Purity:98% Package:1KG;10KG;50KG
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Products Intro: Product Name:2,2'-BIPYRIDINE-5-CARBOXYLIC ACID
CAS:1970-80-5
Purity:99% Package:25kg

2,2'-BIPYRIDINE-5-CARBOXYLIC ACID manufacturers

2,2'-BIPYRIDINE-5-CARBOXYLIC ACID Basic information
Product Name:2,2'-BIPYRIDINE-5-CARBOXYLIC ACID
Synonyms:2,2'-BIPYRIDINE-5-CARBOXYLIC ACID;6-(2-pyridyl)nicotinic acid;6-pyridin-2-ylpyridine-3-carboxylic acid;6-(Pyridin-2-yl)nicotinic acid;2,2Bipyridyl-5-carboxylic acid;5-Carboxy-2,2'-bipyridine;BIPY443, 5-Carboxy-2,2'-bipyridine;2,2'-Bipyridine-5-carboxylic acid 95%
CAS:1970-80-5
MF:C11H8N2O2
MW:200.19
EINECS:
Product Categories:Carboxylic Acids;Pyridines;Carboxylic Acids
Mol File:1970-80-5.mol
2,2'-BIPYRIDINE-5-CARBOXYLIC ACID Structure
2,2'-BIPYRIDINE-5-CARBOXYLIC ACID Chemical Properties
Melting point 218-220 °C
Boiling point 405.5±35.0 °C(Predicted)
density 1.302±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
form powder
pka2.44±0.10(Predicted)
color White
InChIInChI=1S/C11H8N2O2/c14-11(15)8-4-5-10(13-7-8)9-3-1-2-6-12-9/h1-7H,(H,14,15)
InChIKeyLWMHPOLRJIRLPN-UHFFFAOYSA-N
SMILESC1(C2=NC=CC=C2)=NC=C(C(O)=O)C=C1
Safety Information
HS Code 2916399090
MSDS Information
2,2'-BIPYRIDINE-5-CARBOXYLIC ACID Usage And Synthesis
Application2,2'-BIPYRIDINE-5-CARBOXYLIC ACID is a useful research chemical.
Synthesis
[2,2'-Bipyridine]-5-carboxylic acid, methyl ester

58792-53-3

2,2'-BIPYRIDINE-5-CARBOXYLIC ACID

1970-80-5

General procedure for the synthesis of [2,2'-bipyridine]-5-carboxylic acid from methyl [2,2'-bipyridine]-5-carboxylate: first, 2-chloro-5-methoxycarbonylpyridine (1.3 g, 7.6 mmol) was dissolved in 20 ml of mesitylene, PdCl2(PPh3)2 (0.27 g, 0.04 mmol) and 2-trimethylpyridine (2.1 g, 8.6 mmol). The mixture was heated to reflux for 20 hours. After completion of the reaction, it was left to cool, diluted with ether and filtered through a neutral alumina column. The filtrate was washed several times with water and dried with anhydrous sodium sulfate. After evaporation of the solvent, it was purified by silica gel column chromatography to give 1.13 g of compound 10 as a white solid in 70% yield. Subsequently, compound 10 (1.13 g, 5.3 mmol) was suspended in 120 ml of ethanol/water mixed solvent in the ratio of 1:120 and a solution prepared by dissolving KOH (0.35 g, 6.3 mmol) in 2 ml of water was added and the reaction was stirred for 3 hours. After completion of the reaction, the ethanol was removed by distillation and concentration and adjusted to neutral by adding 1 mol/L hydrochloric acid. The resulting suspension was extracted three times with chloroform, the extract was washed with water, dried with anhydrous sodium sulfate and distilled to remove the solvent. The crude product was purified by silica gel column chromatography to afford 0.8 g of compound 11 as a light yellow solid in 75% yield.

References[1] Organic Letters, 2007, vol. 9, # 26, p. 5333 - 5336
[2] Angewandte Chemie - International Edition, 2012, vol. 51, # 32, p. 8097 - 8100
[3] Tetrahedron, 2013, vol. 69, # 14, p. 3019 - 3026
[4] Journal of Organic Chemistry, 1999, vol. 64, # 3, p. 1015 - 1021
[5] Patent: JP6081152, 2017, B2. Location in patent: Paragraph 0015; 0037; 0038
2,2'-BIPYRIDINE-5-CARBOXYLIC ACID Preparation Products And Raw materials
Raw materials[2,2'-Bipyridine]-5-carboxylic acid, methyl ester-->Water-->Potassium hydroxide-->Ethanol
Tag:2,2'-BIPYRIDINE-5-CARBOXYLIC ACID(1970-80-5) Related Product Information
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