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4-Hydroxy-1-methyl-2(1H)-quinolinone, also known as paracetamol, is a commonly used analgesic and antipyretic drug.
It is widely used to relieve pain and reduce fever, and it is also used in the treatment of other conditions such as colds and flu.
In the chemical industry, 4-hydroxy-1-methyl-2(1H)-quinolinone is used as an intermediate in the production of a variety of chemicals and pharmaceuticals.
There are several synthetic routes that can be used to produce 4-hydroxy-1-methyl-2(1H)-quinolinone, each with its own advantages and disadvantages.
The choice of synthetic route depends on factors such as the availability of starting materials, the desired yield and purity of the product, and the cost of the process.
One of the most common synthetic routes for producing 4-hydroxy-1-methyl-2(1H)-quinolinone is the conversion of 4-methylumbelliferone, a naturally occurring compound found in the roots of the shrub Duboisia myoporoides, to 4-hydroxy-1-methyl-2(1H)-quinolinone.
This process involves several steps, including the conversion of 4-methylumbelliferone to 4-methyl-2-oxo-1,2-dihydroquinoline-3-carboxylic acid, the condensation of the carboxylic acid with 2-amino-1,3-propanediol, and the reduction of the resulting amide using hydrogenation or other reducing agents.
Another synthetic route for producing 4-hydroxy-1-methyl-2(1H)-quinolinone involves the reduction of 4-methoxy-1,2-benzenediol, a compound that can be obtained from 4-methylumbelliferone through a series of chemical reactions.
This process involves the reduction of 4-methoxy-1,2-benzenediol to 4-hydroxy-1-methyl-2(1H)-quinolinone using reducing agents such as lithium aluminum hydride or hydrogen in the presence of a catalyst such as palladium on barium sulfate.
Yet another synthetic route for producing 4-hydroxy-1-methyl-2(1H)-quinolinone involves the condensation of salicylaldehyde with acetone to form an acetal, followed by dehydration of the acetal to form 4-hydroxy-1-methyl-2(1H)-quinolinone.
This process is relatively simple and can be performed using commonly available starting materials, but the yield of the product may be lower than with other synthetic routes.
In addition to the above synthetic routes, 4-hydroxy-1-methyl-2(1H)-quinolinone can also be produced using other methods such as the reduction of 4-hydroxy-1-methyl-2-(1H)-quinolinone using hydrogen in the presence of a noble metal catalyst or the reduction of 4-methyl-2-oxo-1,2-dihydroquinoline-3-carboxylic acid using borohydride reagents.
In conclusion, there are several synthetic routes that can be used to produce 4-hydroxy-1-methyl-2(1H)-quinolinone, each with its own advantages and disadvantages.
The choice of synthetic route depends on factors such as the availability of starting materials, the desired yield and purity of the product, and the cost of the process.
The synthetic routes described above are commonly used in the chemical industry and are important for the production of a variety