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The production process of 4-[3-(4-hydroxybutyl)-4,4-dimethyl-2,5-dioxo-1-imidazolidinyl]-2-(trifluoromethyl)benzonitrile, also known as Olodaterol, is a complex and multi-step process that involves the synthesis of several intermediate compounds.
The final product is an important ingredient in the treatment of respiratory diseases, and its production process involves the use of various chemicals, reagents, and equipment.
The production process of Olodaterol can be broadly divided into four stages: synthesis of the intermediate compound, hydrolysis of the intermediate compound, condensation of the intermediate compound, and purification of the final product.
Synthesis of Intermediate Compound:
The synthesis of the intermediate compound involves the reaction of several chemicals, including 4-butanol, 4-chloromethyl-2,5-dioxo-1,3-oxazolidin-3-one, and 2,6-dimethylphenylamine.
The reaction is carried out in a suitable solvent, such as dimethylformamide or acetonitrile, under controlled conditions, such as temperature and pressure.
The use of high-quality raw materials and the control of reaction conditions are critical for the production of a high-quality intermediate compound.
Hydrolysis of Intermediate Compound:
The intermediate compound is then subjected to a hydrolysis reaction, which involves the cleavage of the imide group.
This reaction is carried out in the presence of a strong acid, such as hydrochloric acid or sulfuric acid, and a suitable solvent, such as water or ethanol.
The use of the appropriate solvent and acid concentration is important for the efficient and complete hydrolysis of the intermediate compound.
Condensation of Intermediate Compound:
The next step in the production process is the condensation of the intermediate compound, which involves the formation of the final product, Olodaterol.
This reaction is carried out in the presence of a condensing agent, such as dicyclohexylcarbodiimide or hydroxyquinoline, and a suitable solvent, such as dichloromethane or acetonitrile.
The use of a suitable condensing agent and solvent is critical for the efficient and complete condensation of the intermediate compound.
Purification of Final Product:
The final step in the production process is the purification of the final product, Olodaterol.
This involves the removal of any impurities that may be present in the final product, including unwanted chemicals and by-products.
This process is carried out using suitable purification techniques, such as crystallization, chromatography, or recrystallization.
The use of high-quality purification techniques is important for the production of a high-purity final product.
In conclusion, the production process of Olodaterol involves the synthesis of an intermediate compound, its hydrolysis, condensation, and purification to yield the final product.
The use of high-quality raw materials, controlled reaction conditions, and suitable purification techniques is critical for the production of a high-quality and effective treatment for respiratory diseases.