-
Categories
-
Pharmaceutical Intermediates
-
Active Pharmaceutical Ingredients
-
Food Additives
- Industrial Coatings
- Agrochemicals
- Dyes and Pigments
- Surfactant
- Flavors and Fragrances
- Chemical Reagents
- Catalyst and Auxiliary
- Natural Products
- Inorganic Chemistry
-
Organic Chemistry
-
Biochemical Engineering
- Analytical Chemistry
-
Cosmetic Ingredient
- Water Treatment Chemical
-
Pharmaceutical Intermediates
Promotion
ECHEMI Mall
Wholesale
Weekly Price
Exhibition
News
-
Trade Service
3-Pyridazinecarboxaldehyde, 6-chloro- (9CI) is a compound that has been widely used in various chemical reactions and synthesis methods in the chemical industry.
It is a versatile intermediate that can be synthesized through various chemical routes.
In this article, we will discuss the synthetic routes of 3-Pyridazinecarboxaldehyde, 6-chloro- (9CI) in the chemical industry.
- Hydrolysis of N-chloramine
One of the most common methods for synthesizing 3-Pyridazinecarboxaldehyde, 6-chloro- (9CI) is through the hydrolysis of N-chloramine.
This process involves the reaction of chloramine with a primary or secondary amine in the presence of a strong acid catalyst.
The reaction results in the formation of N-chloramine, which can then be hydrolyzed to produce 3-Pyridazinecarboxaldehyde, 6-chloro- (9CI).
The hydrolysis of N-chloramine is a simple and efficient method for synthesizing 3-Pyridazinecarboxaldehyde, 6-chloro- (9CI) as it uses readily available reagents and does not require specialized equipment.
The reaction can be carried out at room temperature and is highly exothermic, so it is important to take safety precautions when handling the reactants and products.
- Reduction of N-chlorosuccinimide
Another method for synthesizing 3-Pyridazinecarboxaldehyde, 6-chloro- (9CI) is through the reduction of N-chlorosuccinimide.
This process involves the reduction of N-chlorosuccinimide using hydrogen gas in the presence of a reducing agent, such as lithium aluminum hydride (LiAlH4).
The reduction results in the formation of 3-Pyridazinecarboxaldehyde, 6-chloro- (9CI), which can be used as an intermediate in various chemical reactions.
The reduction of N-chlorosuccinimide is a versatile method for synthesizing 3-Pyridazinecarboxaldehyde, 6-chloro- (9CI) as it can be performed using mild conditions and readily available reagents.
The reaction can be carried out at room temperature and does not require specialized equipment, making it a cost-effective and efficient method for synthesizing this compound.
- Direct Chlorination of Pyridazine
3-Pyridazinecarboxaldehyde, 6-chloro- (9CI) can also be synthesized directly from pyridazine through the process of direct chlorination.
This process involves the reaction of pyridazine with chlorine gas in the presence of a catalyst, such as ferric chloride (FeCl3).
The reaction results in the formation of 3-Pyridazinecarboxaldehyde, 6-chloro- (9CI) as well as other byproducts.
The direct chlorination of pyridazine is a simple and efficient method for synthesizing 3-Pyridazinecarboxaldehyde, 6-chloro- (9CI), however, it requires specialized equipment and is more hazardous than other synthetic routes due to the use of chlorine gas.
In conclusion, 3-Pyridazinecarboxaldehyde, 6-chloro- (9CI) is a versatile intermediate that can be synthesized through various chemical routes.
The most common methods include the hydrolysis of N-chloramine, the reduction of N-chlorosuccinimide, and the direct chlorination of pyridazine.
Each method has its own advantages