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2-Nitro-4-pyridinol, commonly referred to as N4PY, is a versatile chemical compound that is widely used in various applications in the chemical industry.
The synthetic routes for N4PY can be broadly classified into four categories: direct nitration of pyridine, nitration of quinoline, nitration of isatin and nitration of salicylaldehyde.
Direct Nitration of Pyridine:
The most straightforward method of synthesizing N4PY is through direct nitration of pyridine.
In this process, pyridine is treated with nitric acid to produce N4PY.
The reaction is typically carried out in the presence of a solvent such as water or acetonitrile, and the reaction is typically complete within 2-3 hours.
The yield of the reaction can be significantly increased by using a catalyst such as sulfuric acid or nitric acid.
Nitration of Quinoline:
Another common method of synthesizing N4PY is through nitration of quinoline.
In this process, quinoline is treated with nitric acid to produce N4PY.
The reaction is typically carried out in the presence of a solvent such as water or acetonitrile, and the reaction is typically complete within 2-3 hours.
The yield of the reaction can be significantly increased by using a catalyst such as sulfuric acid or nitric acid.
Nitration of Isobenzofuran:
Nitration of isobenzofuran, another aromatic compound, can also be used to synthesize N4PY.
In this process, isobenzofuran is treated with nitric acid to produce N4PY.
The reaction is typically carried out in the presence of a solvent such as water or acetonitrile, and the reaction is typically complete within 2-3 hours.
The yield of the reaction can be significantly increased by using a catalyst such as sulfuric acid or nitric acid.
Synthetic Route II:
Methylation of Nitrochloride:
Methylation of nitrochloride, another common synthetic route for N4PY, involves the reaction of methyl iodide with nitrochloride to produce N4PY.
The reaction is typically carried out in the presence of a solvent such as THF or DMF, and the reaction is typically complete within 1-2 hours.
This method is less commonly used due to the high cost of the starting material and the requirement for specialized equipment.
Synthetic Route III:
Oxidation of Salicylaldehyde:
N4PY can also be synthesized through the oxidation of salicylaldehyde.
In this process, salicylaldehyde is treated with oxidizing agents such as potassium permanganate or sodium hypochlorite to produce N4PY.
The reaction is typically carried out in the presence of a solvent such as water or acetonitrile, and the reaction is typically complete within 1-2 hours.
This method is less commonly used due to the high cost of the starting material and the requirement for specialized equipment.
Synthetic Route IV:
Nitration of Phenol:
N4PY can also be synthesized through nitration of phenol.
In this process, phenol is treated with nitric acid to produce N4PY.
The reaction is typically carried out in the presence of a solvent such as water or acetonitrile, and the reaction is typically complete within 2-3 hours.
The yield of the reaction can be significantly increased by using a catalyst such as sulfuric acid or nitric acid.
Conclusion:
In conclusion, the synthetic routes for 2-nit