-
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
5-Chloro-2-hydroxypyrazine is an important intermediate in the production of various chemicals and pharmaceuticals.
It can be synthesized through several routes in the chemical industry.
In this article, we will discuss some of the most commonly used synthetic routes for the preparation of 5-chloro-2-hydroxypyrazine.
- Hydrolysis of Chloroacetophenone
One of the most common methods for the synthesis of 5-chloro-2-hydroxypyrazine is the hydrolysis of chloroacetophenone.
Chloroacetophenone can be synthesized by the reaction of acetophenone and chloroform.
The hydrolysis of chloroacetophenone is carried out by treating the compound with water.
The reaction is exothermic, and it produces 5-chloro-2-hydroxypyrazine as a white solid.
- Reduction of 2-Nitro-5-chloropyrazine
Another route for the synthesis of 5-chloro-2-hydroxypyrazine is the reduction of 2-nitro-5-chloropyrazine.
2-Nitro-5-chloropyrazine can be synthesized by the nitration of 2-aminopyrazine.
The reduction of 2-nitro-5-chloropyrazine can be carried out by treating the compound with hydrogen in the presence of a catalyst such as palladium on barium oxide.
This reaction also produces 5-chloro-2-hydroxypyrazine as a white solid.
- Decarboxylation of 5-Chloro-2-aminopyrazine Carboxylic Acid
5-Chloro-2-hydroxypyrazine can also be synthesized by the decarboxylation of 5-chloro-2-aminopyrazine carboxylic acid.
5-Chloro-2-aminopyrazine carboxylic acid can be synthesized by the reaction of 5-chloro-2-aminopyrazine with sodium hydroxide.
The decarboxylation of the carboxylic acid is carried out by treating the compound with carbon dioxide.
This reaction produces 5-chloro-2-hydroxypyrazine as a white solid.
- Hydrolysis of 5-Chloro-2-nitropyrazine
5-Chloro-2-hydroxypyrazine can also be synthesized by the hydrolysis of 5-chloro-2-nitropyrazine.
5-Chloro-2-nitropyrazine can be synthesized by the nitration of 2-aminopyrazine.
The hydrolysis of 5-chloro-2-nitropyrazine is carried out by treating the compound with water.
This reaction also produces 5-chloro-2-hydroxypyrazine as a white solid.
In conclusion, the synthesis of 5-chloro-2-hydroxypyrazine is a relatively simple process, and there are several routes to synthesize this compound.
The most commonly used methods include the hydrolysis of chloroacetophenone, the reduction of 2-nitro-5-chloropyrazine, the decarboxylation of 5-chloro-2-aminopyrazine carboxylic acid, and the hydrolysis of 5-chloro-2-nitropyrazine.
The choice of synthesis route depends on the availability of starting materials and the desired yield of the final product.